ANNUAL MEETING 2016 September 19 & 20 THE WESTIN KIERLAND SCOTTSDALE, AZ PCMA Members The Pharmaceutical Care Management Association is the national association representing America’s pharmacy benefit managers. PBMs administer prescription drug plans for more than 266 million Americans with health coverage provided through Fortune 500 employers, health insurance plans, labor unions, and Medicare Part D. Welcome to the PCMA Annual Meeting 2016 The PCMA Annual Meeting is the industry’s premier executive conference. The event is tailored specifically for senior executives from PBMs and their affiliated business partners — most notably drug manufacturers. We’ve designed the Annual Meeting to be an important part of your business strategy and are proud of the unique value that the conference offers to PBM, specialty pharmacy and pharma industry executives. The decision makers in attendance, educational insights, and business opportunities are ultimately what make the Annual Meeting so valuable. There are many pressing issues impacting the health care industry today, key among them are innovation and affordability, access and value. These and many other issues will be addressed both on and off the stage during the next two days. The interaction and dialogue that takes place at this event serves to promote continued industry collaboration addressing the many challenges we face. We thank you for coming to this year’s Annual Meeting. We hope that you find your time spent to be enlightening and beneficial to your business. Enjoy your time in Scottsdale. Contents 2Schedule-at-a-Glance 29 PCMA Board of Directors 5Maps 30 PCMA Staff 8 General Information 31 PCMA Members 9 Session Details 32 2016 PCMA Affiliates 33 Conference Sponsors 19Speakers 1 Schedule-at-a-Glance MONDAY, SEPTEMBER 19 7:00 am – 7:00 pm Registration Open Culturekeepers Hall West 7:00 am – 6:30 pm Private Meeting Rooms Open 7:30 am – 9:00 am Networking Breakfast Trailblazer C 9:00 am – 12:00 pm GENERAL SESSIONS Kierland Grand 2/3 9:00 am – 9:15 am Welcome Conference Moderator: Betty Nguyen, Anchor and Journalist, NBC News & MSNBC 9:15 am – 9:45 am How PBMs Deliver Clinical Value Through Specialty Pharmacy Alan Lotvin, Executive Vice President, CVS/specialty, CVS Health 9:45 am – 10:15 am The World of Pharmacy and Pharmaceuticals in 2030 Bill Roth, Founding Partner, Blue Fin Group 10:15 am – 11:00 am Value-based Contracting: U.S. Landscape Realities Jim Clement, Executive Director, Cost of Care and Supply Chain Strategy, Aetna Pharmacy Management, Aetna Mike Ryan, Senior Vice President, U.S. Value, Access and Policy, Bristol-Myers Squibb Moderator: Tom Knox, President, Fathom Healthcare Solutions 11:00 am – 11:30 am Policy Trends to Watch in 2017 Larry Kocot, Principal and National Leader, Center for Healthcare Regulatory Insight, KPMG 11:30 am – 12:00 pm The Business of BioPharma: Building a Healthy Future for Patients, Payers and Society George Scangos, Chief Executive Officer, Biogen Moderator: Jerry Miller, President, J. Miller Consulting 12:15 pm – 1:45 pm Member Company Lunch Receptions Aetna: Kierland Grand 1B Humana Pharmacy Solutions: Trailblazer DE MedImpact: Kierland Grand 1C OptumRx: Trailblazer C Networking Lunch: Kierland Grand 1A and Culturekeepers Hall West 2 Schedule-at-a-Glance 1:45 pm – 6:30 pm Afternoon is open for private meetings and networking 6:30 pm – 9:00 pm Cocktail and Dinner Reception with Live Music Northern Sky Terrace TUESDAY, SEPTEMBER 20, 2016 7:00 am – 4:00 pm Registration Open Culturekeepers Hall West 7:00 am – 8:00 pm Private Meeting Rooms Open 7:00 am – 8:45 am Networking Breakfast Trailblazer C 8:45 am – 11:45 am GENERAL SESSIONS Kierland Grand 2/3 8:45 am – 9:45 am PCMA Leadership Session The Political and Policy Environment Mark Merritt, President & Chief Executive Officer, PCMA The PBM/Pharma Relationship in the Era of High Price Drugs William Fleming, Segment Vice President, Humana Inc. & President, Humana Pharmacy Solutions Tim Wentworth, President & Chief Executive Officer, Express Scripts Moderator: Kent Rogers, Senior Vice President, Industry Relations, OptumRx 9:45 am – 10:30 am Challenges Related to Outcomes Contracting in the U.S. and Solutions for Addressing Them Chris Bradbury, Leader, Integrated Clinical Solutions and Specialty Pharmacy, Cigna Pharmacy Management, Cigna Claudio Faria, Senior Director, U.S. Health Economics Outcomes Research, Celgene Pierre Leurent, Chief Executive Officer, President of the Management Board & Founder, Voluntis Moderator: Eric Elliott, Chief Executive Officer, LMK Advisory & Chairman, Voluntis 10:30 am – 11:00 am ACOs and IDNs: Understanding Payer Moves Toward Value-based and Outcomes Contracting Charles Kennedy, Vice President & Chief Medical Officer for Clinical Integration, Aetna 11:00 am – 11:45 pm Perspectives from Wall Street George Hill, Director, Deutsche Bank Bob Jones, Vice President, Goldman Sachs & Co. Schedule-at-a-Glance 3 12:00 pm – 1:30 pm Member Company Lunch Receptions CVS Health: Trailblazer DE Express Scripts: Trailblazer C MagellanRx Management: Kierland Grand 1B Prime Therapeutics: Kierland Grand 1C Networking Lunch: Kierland Grand 1A and Culturekeepers Hall West 1:30 pm – 8:00 pm Afternoon is open for private meetings and networking 8:00 pm – 10:00 pm Cocktail and Dessert Reception Lobby Lounge & Terrace Don’t miss these important networking events! Monday 12:15 pm – 1:45 pm Tuesday 12:00 pm – 1:30 pm Monday evening 6:30 pm – 9:00 pm Northern Sky Terrace Cocktail and Dinner Reception Live music, food stations, and views of the lake and golf course provide a relaxed and fun atmosphere, perfect for business networking, during this special reception and dinner. 4 Schedule-at-a-Glance Member Company Lunch Receptions These receptions offer excellent opportunities for interactions between PBM member and drug manufacturers. Manufacturer attendees will flow in and out of the concurrent receptions whereas members are asked to post in their designated room during the reception time. Tuesday evening 8:00 pm – 10:00 pm Lobby Lounge & Terrace Cocktail and Dessert Reception Join your peers for dessert, cocktails, and conversation at an after-dinner reception. Maps LOBBY LEVEL Explorers Terrace B Tribal A B Mapmakers Expedition Hall Pathfinders A Merriam A B Whipple A B The Rim Bar Scotch Library Lobby Lounge A A A Trailblazers Terrace Lowell B Powell Cushing A Trailblazers West Sitgreaves Discovery Hall Parke Stargazers Terrace B B E B Trailblazers South Hall Of State Concierge Coffee Flats & Snowbowls Entry Toonerville 66 Trading Post Front Desk 1A 1B 1C 2 Vista Morada Patio Activities listed in the schedule-at-a-glance Culturekeepers Hall West Kierland Grand Ballroom Private meetings rooms Shared meeting rooms 3 4A 4B 4C 2087 DD 2085 DD 2083 DD 2081 TK 2086 TD 2084 TK 2082 TK CL 2088 TKA CL 2089 DD 2120 TD 2090 TK 2118 TK 2119 TD 2091 DD 2117 TK 2092 TDA 2116 TD 2093 DD 2114 TK 2115 TD 2094 TK 2112 TD 2113 TK 2095 DD 2110 TK 2111 TD 2096 TD 2108 TD 2109 DK 2097 DK 2106 TD 2107 TD 2098 TK 2105 TD 2099 DK 2100 DK 2101 DD 2102 DD 2103 DK 2104 DK Culturekeepers Hall South 2121 TK 2122 TK 2123 TD 2124 TK 2125 TD COURTYARD EXIT Tangent FedEx Business Center D C To additional meeting rooms Kierland Mining Co. Trailblazers Ballroom To Lobby Maps 5 LOWER LEVEL Northern Sky Terrace Terrace Terrace Terrace Billiards Waltz & Weiser Cantina Activities listed in the schedule-at-a-glance Private meetings rooms 6 Maps B C Greenway A 2 Herberger Ballroom A 4 1 3 B 5 West Foyer A B Kirkland Noble Terrace Dreamweavers Canyon Private Dining Muddle Bar Private Dining Shared meeting rooms Rainmakers Ballroom Visionaries Hall Terrace Nellie Cashman’s Monday Club Cafe East Foyer North Foyer Deseo Enhance Your Conference Experience View the list of who’s attending Message with other attendees Review the agenda and create a personalized schedule Access hotel maps and meeting room locations Stay informed of any lastminute schedule changes Check out the sponsors Download our NEW app for access on the go! Stop by the reg desk if you need help downloading the app. General Information Registration Desk Hours Presentations The PCMA registration desk will be open in Culturekeepers Hall West each day of the conference during the hours listed below. Should you have any questions, please stop by the registration desk and staff will be able to assist you. Presentations authorized for distribution will be posted online and in the conference app after the conference. Attendees will be notified by email once presentations are available. Sunday, September 18 4:00 pm – 7:00 pm Monday, September 19 7:00 am – 7:00 pm Tuesday, September 20 7:00 am – 4:00 pm Photography Professional photographs taken during the conference may be posted online and/or printed in future materials. Disclaimer If you require a copy of your registration confirmation, receipt of payment, or invoice, please email Diane Fulton, [email protected]. The opinions expressed by program participants are those of the individual presenters. They do not necessarily reflect the views of PCMA or its members. Security Attendance at a Pharmaceutical Care Management Association (PCMA) meeting or event includes the limited, non-exclusive, revocable, and nontransferable right and license to use any PCMA materials, whether written, oral or electronic, made available by PCMA to the attendees for informational or personal use purposes only. PCMA reserves all other rights. PCMA or its licensors own all rights in and to all of its presentations, content, designs, methodologies, processes, programs, products, information, and documentation. PHARMACEUTICAL CARE MANAGEMENT ASSOCIATION, PCMA and all other names, logos, and icons identifying PCMA and its products and services are proprietary trademarks of PCMA, and any use of such marks without the express written permission of PCMA is strictly prohibited. In order to provide a secure environment, conference participants MUST wear name badges when attending any conference function, including sessions, meals, evening receptions, and private meetings in member and sponsor meeting room facilities. Security will monitor entrances to all conference activities. Please do not misplace or forget badges, as duplicates will not be provided. Neon orange badges indicate drug manufacturers. Beige badges indicate PBM, payer, specialty pharmacy, and other industries. Shuttle Transportation Shuttle service is provided to and from Marriott McDowell Mountain on Monday and Tuesday every 15 minutes beginning on the hour at 6:00 am and ending at 10:00 pm from the following locations: »» The Westin Kierland: South Terrace, just outside the Kierland Grand Ballroom »» Marriott McDowell Mountain: Main Entrance Internet Complimentary Wi-Fi is available throughout the Westin Kierland and in the guestrooms. In the conference center and meeting rooms, please use the password pcmaAM2016 to access the Wi-Fi. It can be accessed without a password while in the lobby and other public spaces. 8 General Information SESSION DETAILS Session Details Session Details Monday, September 19 9:15 am – 9:45 am Kierland Grand 2/3 How PBMs Deliver Clinical Value Through Specialty Pharmacy Alan Lotvin, Executive Vice President, CVS/specialty, CVS Health Pharmacy benefits are, first and foremost, about helping patients manage their conditions. Specialty pharmacies and PBMs are applying their expertise and assets toward progressive solutions to help their clients support the clinical needs of patients while managing costs. All major specialty pharmacies offer many valuable solutions in regards to managing REMS, patient adherence, and drug delivery. However, patients and payers realize the most savings and clinical value when specialty pharmacies and PBMs combine. This session will highlight the value payers and patients receive, such as indication-based solutions, managing utilization across benefits, and a robust approach to supporting patients beyond adherence, with a specialty pharmacy/PBM relationship. Combined, all of these approaches help support patient care and control overall specialty costs rather than a singular focus on drug costs or costs associated with specialty drug non-adherence. Session Details 9 Monday, September 19 9:45 am – 10:15 am Kierland Grand 2/3 The World of Pharmacy and Pharmaceuticals in 2030 Bill Roth, Founding Partner, Blue Fin Group This session will explore a broad view of where our industries are headed in regard to innovation, the business models we’ll need to support it, and the importance of our alignment in order to balance society’s priorities. Combining the view of the cost of health care spiraling to $4.4 trillion by the end of the decade, with continued innovation on the way in the areas of proteonomics, genomics and precision medicine, biosynthetics, AI, and more, Bill will explore likely scenarios for how they could impact our own strategies as manufacturers, payers and consumers. 10 Session Details Monday, September 19 10:15 am – 11:00 am Kierland Grand 2/3 Value-based Contracting: U.S. Landscape Realities Jim Clement, Executive Director, Cost of Care and Supply Chain Strategy, Aetna Pharmacy Management, Aetna Mike Ryan, Senior Vice President, U.S. Value, Access and Policy, Bristol-Myers Squibb Moderator: Tom Knox, President, Fathom Healthcare Solutions Though still in their infancy in the U.S. health care system, value-based risk sharing agreements are growing in popularity. Market forces have been driving stakeholders to explore new types of financing and access, shifting risk towards value, indications, and/or outcomes-based arrangements. These varying types of value-based arrangements have different goals and metrics for success. Some might allow a payer to minimize risk or manage risk differently; others allow manufactures to create product differentiation and to potentially obtain the full value of the product; while others still might allow for population versus patient management and improved data repositories and informatics systems. Success depends on good contract design, availability of data, and administration. During this session the panel will discuss the pros and cons of value-based contracts from their varying perspectives. Some of the questions they will address include what’s driving the demand for these types of contracts, how are players looking at specialty versus non-specialty therapies as candidates for these arrangements, what are some of the barriers to doing value-based contracts in the current U.S. landscape, what are the manufacturer versus payer expectations of one another in engaging in these agreements, and finally, how do they see these arrangements evolving over time and with greater adoption. Session Details 11 Monday, September 19 11:00 am – 11:30 am Kierland Grand 2/3 Policy Trends to Watch in 2017 Larry Kocot, Principal and National Leader, Center for Healthcare Regulatory Insight, KPMG Driven by the high cost of drugs, the prescription drug industry, including PBMs, is being discussed in Washington DC and State capitols at a level not seen in recent years. New proposals for legislative and regulatory reform seem to come each day. In this environment it can be difficult to decipher what legislative and regulatory policy actions are happening now and in the near future that will directly impact our business. During this session Larry will discuss a number of policy trends that will impact healthcare markets in the next year, with specific implications for PBMs and pharmaceutical manufacturers. 12 Session Details Monday, September 19 11:30 am – 12:00 pm Kierland Grand 2/3 The Business of BioPharma: Building a Healthy Future for Patients, Payers and Society George Scangos, Chief Executive Officer, Biogen Moderator: Jerry Miller, President, J. Miller Consulting The biopharma industry is currently in an historic period of innovation, with deep pipelines across many difficult-totreat disease areas. However, there are numerous challenges that may impact whether promising drug candidates ever get to the patients who need them. As the CEO of Biogen and the current Chairman of PhRMA, Dr. Scangos has a unique view into the challenges of drug development, the current policy environment and the appropriate balance between innovation, access, and cost. Session Details 13 Tuesday, September 20 8:45 am – 9:45 am Kierland Grand 2/3 PCMA Leadership Session The Political and Policy Environment Mark Merritt, President & Chief Executive Officer, PCMA The PBM/Pharma Relationship in the Era of High Price Drugs William Fleming, Segment Vice President, Humana Inc. & President, Humana Pharmacy Solutions Tim Wentworth, President & Chief Executive Officer, Express Scripts Moderator: Kent Rogers, Senior Vice President, Industry Relations, OptumRx The high cost of drugs is an unavoidable subject for the PBM/payer and pharma industries today. The drug pipeline of recent years has brought us breakthrough therapies that are delivering tremendous value to our health care system, albeit at high prices. At the same time, we’re experiencing high costs associated with drugs offering little incremental value, and irresponsible pricing practices from bad actors in the industry. These and many other factors are contributing to a business and political environment that threatens the ability to reward innovation in the pharma industry, and continue the use of free market solutions that our system has benefited from for so long. Our industries share a common goal, the sustainability of the free market health care system that rewards innovation and improved outcomes and the lives of patients. During this session, the outgoing and incoming PCMA Board Chairmen will share their views on industry trends, the PBM value proposition, and the evolving relationship between manufacturers and PBMs. 14 Session Details Tuesday, September 20 9:45 am – 10:30 am Kierland Grand 2/3 Challenges Related to Outcomes Contracting in the U.S. and Solutions for Addressing Them Chris Bradbury, Leader, Integrated Clinical Solutions and Specialty Pharmacy, Cigna Pharmacy Management, Cigna Claudio Faria, Senior Director, U.S. Health Economics Outcomes Research, Celgene Pierre Leurent, Chief Executive Officer, President of the Management Board & Founder, Voluntis Moderator: Eric Elliott, Chief Executive Officer, LMK Advisory & Chairman, Voluntis During yesterday’s session we heard about the realities of the landscape for value-based contracts. While these types of contracts offer many opportunities, there are also significant difficulties in getting these contracts to the desired design and final stage. This panel will explore some of the biggest challenges and solutions for these contracting approaches — including the varying payer needs for an individual product, the high level of specificity needed, and data collection. Helping to frame this conversation are three individuals, two from well-known companies with a clear view for how they could work and one from a company with capabilities and a business model to help solve one (hopefully last) hurdle on our way to extensive penetration of outcomes based contracts. Session Details 15 Tuesday, September 20 10:30 am – 11:00 am Kierland Grand 2/3 ACOs and IDNs: Understanding Payer Moves Toward Value-based and Outcomes Contracting Charles Kennedy, Vice President & Chief Medical Officer for Clinical Integration, Aetna Hospitals, physician practices, and long term care facilities are continuing to consolidate under Integrated Delivery Networks (IDNs). Like the rest of the industry, health system reimbursement practices are moving towards outcomes and value-based care. There are currently two major themes in the evolution of health care payment methodologies: increasing accountability for both quality and total cost of care, and a greater focus on population health management as opposed to payment for specific services. Moreover, CMS’s strategy — to increasingly link physician financial reward to the value of the services they provide in keeping individuals and populations healthy — opens the door to structural re-alignment of health care delivery. These advanced alternative payment models come with substantial risk elements. During this session, Dr. Kennedy will talk in detail about the challenges in aligning individualized value-based decision making and population based payment. He will share case studies demonstrating why individual, value-based analytics matter, and he will provide examples of newly available electronic patient datasets combined with new analytic frameworks that can result in successful health care knowledge bases that make the individual consumer centric experience a reality. Finally, he will share his perspectives on the role of pharma in this evolving reimbursement landscape. 16 Session Details Tuesday, September 20 11:00 am – 11:45 am Kierland Grand 2/3 Perspectives from Wall Street George Hill, Director, Deutsche Bank Bob Jones, Vice President, Goldman Sachs & Co. Due to their unique vantage point, Wall Street analysts offer a distinctive perspective of our industries. During this session, George and Bob will share their thoughts on the most important trends impacting the intersection of PBMs and manufacturers. Some of the ideas that will be addressed include: »» Impact of managed care consolidation; »» Thoughts on channel consolidation; »» Thoughts on industry pricing structures and models; »» The value proposition PBMs are making to their clients around clinical management and specialty pharmacy — outcomes and indication-based contracts; »» Formulary consolidation; »» ePA process and how PAs impact manufactures; and »» Biosimilars. Session Details 17 18 Session Details SPEAKERS Speakers Speakers Chris Bradbury Leader, Integrated Clinical Solutions and Specialty Pharmacy, Cigna Pharmacy Management Cigna Chris Bradbury is currently the Integrated Clinical Solutions and Specialty Pharmacy Leader within Cigna Pharmacy Management. He serves as an Executive Committee member of Cigna Pharmacy, one of the nation’s largest pharmacy benefit managers and specialty pharmacies. Prior to joining Cigna in 2013, Bradbury spent fifteen years at Medco Health Solutions where he led many of the PBM’s clinical and integrated data patient safety solutions as well as the population health, chronic care management and care coordination solutions. In addition, he served as a management consultant focused on business strategy, process reengineering, strategic sourcing, and benchmarking in the healthcare and financial services industries. Bradbury earned his Bachelor of Business Administration in Finance from Georgetown University and earned his Master of Business Administration from MIT’s Sloan School of Management. Jim Clement Executive Director, Cost of Care and Supply Chain Strategy, Aetna Pharmacy Management Aetna As Executive Director of Cost of Care and Supply Chain Strategy for Aetna Pharmacy Management, Jim Clement is responsible for leading Aetna’s enterprise relationships with pharmaceutical manufacturers and setting formulary management strategy. Clement is responsible for all rebate and fee-for-service contracting and administration, specialty and clinical program partnerships and coordination of business-to-business strategies, including international and ACO strategies. Prior to joining Aetna, Clement worked at Genentech in channel and distribution management focusing on the PBM and specialty pharmacy segments and serving as an in-house consultant in forming payer contracting and negotiating strategies. Prior to Genentech, he was the Director of Pharmaceutical Contracting at Express Scripts where he was responsible for rebate contracting and manufacturer relations. Clement is a graduate of the University of Missouri-Columbia and holds a Master of Health Administration from Saint Louis University School of Public Health. Speakers 19 Eric Elliott Chief Executive Officer, LMK Advisory & Chairman, Voluntis Eric Elliott is currently the Chief Executive Officer of LMK Inc, and Chairman of Voluntis. Separately, he is working independently with investors to evaluate potential assets for ownership and leadership. Voluntis is a French-based medical device/software algorithum driven tool that accelerates the effectiveness of medications. Initially targeted at diabetes and oncology, it is being utilized extensively in the E.U. markets, and in some applications in the U.S. It is under FDA review for extended U.S. market release in 2016. Prior to his current roles, Elliott led three organizations operating in the pharmacy benefit management industry. In his most recent role as Prime Therapeutics’ President and Chief Executive Officer (April 2010 - April 2015), he was responsible for all operating and strategic aspects of the full service pharmacy benefit management (PBM) company. With approximately $19 billion in annualized drug spend under management at the time of his departure, Prime was the fourth largest pharmacy benefit manager in the United States. Prime was servicing 23 health plans, other PBMs, and several large employer direct customers. Previously, Elliott held the role of president at Cigna Pharmacy Management (2006-2010) and Aetna Pharmacy Management (2003-2006) With experience running three integrated PBMs, he is skilled in leading and growing businesses, to include line and segment expansions. His aggressive and innovative business leadership is focused on helping clients obtain the maximum value from their pharmacy benefits and enabling individuals to get the critical medicine they need, while creating a work environment that attracts and retains the very best. Under Elliott’s leadership, Prime was recognized locally and nationally by prominent publications and organizations for its employee engagement, healthy workplace, highest quality and care of service for members, and business growth. During his tenure, Prime Therapeutics more than doubled in size and accelerated the value created by the organization more than four fold. Elliott received his bachelor’s degree in Management and Finance, and a Master of Business Administration from Temple University in Philadelphia. He served for many years on the board of directors at Prime, PCMA, and the Twin Cities American Heart Association. He continues to serve on the board of The Main Street America Group and Voluntis. Claudio Faria Senior Director, U.S. Health Economics Outcomes Research Celgene Claudio Faria is the Senior Director, of U.S. Health Economics Outcomes Research for Celgene. In this role he leads U.S. outcomes research and Market Access HEOR customer initiatives. Faria joined Celgene after many years as Director of Oncology at Eisai. He has extensive experience in HEOR in the pharmaceutical industry both in the U.S. and internationally. He also has expertise in the development of product value propositions and in successfully leading teams in delivering value propositions to market access customers and key decision makers. Prior to his experience at Eisai, Faria developed and was Associate Director of Clinical Research and Health Outcomes at the University of Massachusetts Medical School. He was also a Medical Science Liaison at ScheringPlough Corporation and a Senior Research Pharmacist of Investigational Drug Service at Brigham & Women’s Hospital and Dana-Farber Cancer Institute in Boston. Faria has held faculty positions at the Massachusetts College of Pharmacy and Northeastern University. He is also well published in medical literature. 20 Speakers William Fleming Segment Vice President, Humana Inc. President, Humana Pharmacy Solutions Dr. William K. Fleming, PharmD, is Segment Vice President for Humana Inc. and President, Humana Pharmacy Solutions, where he is responsible for Humana’s pharmacy operations and business strategy that services all Humana segments, including its non-Humana membership. Fleming serves on Humana’s Management Team (Segment President). A 22-year Humana rookie, Fleming has spent the majority of his pharmacy career pioneering Humana’s pharmacy business. He has worked in partnership with Humana’s retail segment to deliver an industryleading Part D business. Prior to Humana, he had various opportunities in hospital pharmacy, retail pharmacy, Medicaid pharmacy benefit management, and nuclear pharmacy. Fleming received his BS Pharmacy from the University of Kentucky College of Pharmacy where he went on to receive his Doctor of Pharmacy. He also holds a BA in General Studies from Transylvania University with an emphasis in Biology and Economics. William currently serves on the Board of Directors of PCMA and PQA (the Pharmacy Quality Alliance) and has held prior Board/Trustee appointments to various pharmacy and charity organizations. George Hill Director Deutsche Bank George Hill has more than 15 years of Wall Street experience and more than 17 years of health care industry experience. Hill joined Deutsche Bank in September 2013 as the senior analyst covering health care technology and distribution. Hill previously worked at Citi Research from November 2010 to July 2013 as a senior analyst covering the health care technology and distribution sector. Prior to joining Citi, Hill worked six years at Leerink Swann where he was the senior health care services analyst and also spent time as the senior calling officer for Leerink’s health care services investment banking efforts. Prior to Leerink, Hill worked on the health care services research team at Thomas Weisel Partners and worked as an analyst at Citigroup Asset Management. Before working on Wall Street, Hill worked as a consultant and journalist in the pharmaceutical services sector. Hill received his BA from Rutgers University. Bob Jones Vice President Goldman Sachs & Co. Robert P. Jones joined Goldman Sachs & Co. in April 2008 and was promoted to Vice President in January 2010. Prior to joining the firm, Jones worked at UBS Securities LLC as an Associate Analyst in the generic pharma manufacturers, PBMs, distributors and labs group. He also held previous roles within Johnson & Johnson Company, including Senior Analyst in the strategic planning and business analytics group. Jones graduated from Lehigh University with a Bachelor of Science in Finance in 1999. Speakers 21 Charles Kennedy Vice President & Chief Medical Officer for Clinical Integration Aetna Charles D. Kennedy, MD, is Vice President and Chief Medical Officer for Clinical Integration. In this role, Kennedy is responsible for planning the integration of the Aetna and Humana clinical businesses after the close of the proposed transaction. The primary goal of the Aetna and Humana transaction is to offer consumers a broader choice of products, access to higher quality and more affordable care, and a better overall experience in more geographic locations across the country. Kennedy has a dual reporting relationship to Rick Jelinek, Executive Vice President, Humana Integration, and to Dr. Hal Paz, Executive Vice President, Chief Medical Officer. Previously, Kennedy was Chief Population Health Officer, Healthagen, responsible for leading population health and care management strategies and working with health systems and provider organizations to design and implement population health management programs Kennedy is a recognized expert in health care and health information technology. He was a founding commissioner of the Certification Commission for Health Information Technology (CCHIT), the first organization recognized by the federal government to certify EMRs. He recently concluded a two term commitment as the health insurance industry representative on the HIT Policy Committee, a Federal Advisory Committee that is guiding CMS policies to allocate $40 billion in federal funding for HIT deployment. Kennedy serves on the AHIP Foundation Board of Directors and on the advisory board for the Center for Healthcare Innovation, Healthcare and Life Science Innovation Lab. Kennedy holds an MD in Internal Medicine from the University of California at Los Angeles, an MBA in Corporate Strategy and Health Care Economics from Stanford University, and a bachelor’s degree in Genetics from the University of California at Berkeley. He has been featured and quoted on the topics of health care technology and operations in news publications and outlets that include ComputerWorld, Bloomberg, Associated Press, The Pink Sheet, The Industry Standard, Modern Healthcare, HealthLeaders. Tom Knox President Fathom Healthcare Solutions As President at Fathom Healthcare Solutions Inc., Tom Knox is responsible for leading all market access, reimbursement, and health policy aspects for pharmaceutical, biotech, and medical device organizations. Knox’s long history of cross-functional leadership positions allows him to guide clients in their effort of balancing the complex interplay of payers, health care professionals, and patients. His in-depth knowledge of access and reimbursement will help organizations strengthen the organizational leadership role of managed care functions beyond just being “account” and “contracting” experts. Utilizing a cross-functional stakeholder orientation combined with his experience implementing several integration processes enables Knox to provide companies the ability to quickly re-gain maximum functionality. Prior to starting Fathom Healthcare Solutions, Inc., Knox worked as Vice President, Managed Markets, Health Policy and Government Affairs for Allergan, Inc. During his more than nine years at Allergan, Knox was responsible for strategy and execution related to reimbursement and policy supporting business units in ophthalmology, neurology, urology, medical dermatology, and medical aesthetics. Tom has experience in the development of strategy related to all aspects of Medicare, Medicaid, commercial, specialty pharmacy, and health policy. Prior to Allergan, Knox helped to establish two new businesses, HealthNexis a company founded by Cardinal Health, McKesson and AmeriSourceBergen, and aaiPharma a specialty pharmaceutical company focused on pain management. For 15 years Knox worked at Novartis Nutrition in multiple roles related to sales and marketing, account management and business unit leadership. Tom attended the University of Illinois-Chicago, Cardinal Stritch University and Executive Leadership courses at Harvard University. 22 Speakers Larry Kocot Principal and National Leader, Center for Healthcare Regulatory Insight KPMG S. Lawrence Kocot is a Principal at KPMG, LLP and National Leader of KPMG’s Center for Healthcare Regulatory Insight. The Center follows health care regulatory and policy trends driving health care transformation and industry convergence and the broader implications of operating in a more collaborative and integrated U.S. healthcare payment and delivery environment. Kocot provides strategic advice and counsel to companies on regulatory matters relating to public health care programs, including Medicare and Medicaid. Kocot has served as counsel to a wide range of corporations and associations on a variety of different matters, including investigations by the FTC, DOJ, SEC, and state attorneys general, as well as on qui tam and other litigation. Additionally, Kocot has represented companies in audits and other disputes with the federal government and counseled organizations on the development and formation of accountable care organizations and other alternative payment arrangements. Kocot is a former Senior Advisor to the Administrator of CMS at the U.S. Department of Health and Human Services. In this capacity, he was involved in a wide range of health care policy issues and operations related to Medicare and Medicaid. Notably, Kocot was a key member of the management and operations team responsible for pharmaceutical, pharmacy, and PBM issues, including the launch and operation of the Medicare Prescription Drug Benefit (Part D). More specifically, he led the development of policy and regulation under the Part D program; guided CMS efforts to design and develop new systems functionality for providing beneficiary information to providers in real time at the point of sale, he designed and launched CMS initiatives on pharmacy quality and pharmacy quality alliances, and he supervised pharmaceutical delivery and data management during and after Hurricane Katrina. Prior to joining KPMG, Kocot practiced law at Epstein Becker Green, PC, and Dentons, US LLP. From 2007-2015, Kocot was a visiting fellow in the Economic Studies Program at the Brookings Institution; he was also Deputy Director of the Engelberg Center for Health Care Reform at Brookings from 2007-2013. Kocot was a fellow in International Security Studies at the Center for Strategic and International Studies (CSIS), and an adjunct fellow at CSIS for several years thereafter. Before his government service, Kocot was Senior Vice President and General Counsel at the National Association of Chain Drug Stores, where he was responsible for all legal matters and represented the industry before Congress, state legislatures, and state and federal regulatory agencies. Pierre Leurent Chief Executive Officer, President of the Management Board & Founder Voluntis Pierre has more than 15 years of international experience in software, medical devices, disease management, and telemedicine solutions in Europe and the United States. Before founding Voluntis in 2001, Leurent worked with General Electric Medical Systems and with HealthCenter Internet Services, an online cardiology EMR solution vendor in San Francisco. In addition, Leurent is the Director of Syntec Numérique, where he leads the telemedicine workgroup. He is co-leader of CSIS-CSF’s e-health workgroup and e-health advisor within Nouvelle France Industrielle’s health steering committee. Leurent is a graduate of the Ecole Centrale Paris engineering school. Speakers 23 Alan Lotvin Executive Vice President, CVS/specialty CVS Health Dr. Alan M. Lotvin, MD, is Executive Vice President of Specialty Pharmacy for CVS Health. In this role, Lotvin has overall responsibility for the company’s Specialty Pharmacy business, a rapidly growing division of the company’s pharmacy benefits management business. He is focused on driving specialty pharmacy strategy and identifying opportunities for growth and innovation in this fast-growing segment of the health care industry. Lotvin is a published author with an extensive clinical background and experience in the health care services, pharmaceutical benefit management and specialty pharmacy industries. Prior to joining CVS Health, Lotvin was President and Chief Executive Officer of ICORE Healthcare, a Magellan Health Services company. Previously, he has held roles as President and Chief Operating Officer of M|C Communications, a leading medical education provider. After leaving clinical practice, Lotvin served in various senior management roles at Medco Health Solutions, including serving as President of Medco Specialty Pharmacy Services. Lotvin began his career as an interventional cardiologist in the New York metropolitan area with a faculty appointment at College of Physicians and Surgeons at Columbia University. Lotvin holds a Masters Degree in Medical Informatics from Columbia University and a Medical Degree from the State University of New York Health Sciences Center in Brooklyn. Mark Merritt President & Chief Executive Officer PCMA Mark Merritt is the President and Chief Executive Officer of PCMA, which represents the nation’s PBMs. The PBM industry plays a pivotal role in American health care, administering prescription drug benefits for over 200 million Americans covered by Fortune 500 companies, health insurance plans, labor unions, and Medicare Part D. Before joining PCMA, Merritt played senior roles with America’s Health Insurance Plans (AHIP), the Pharmaceutical Research and Manufacturers of America (PhRMA), and the presidential campaigns of Senators Bob Dole and Lamar Alexander. Merritt also served as a Fellow at Harvard University’s John F. Kennedy School of Government, where he lectured on the intersection of politics, public policy, and the media. Merritt is known for innovative, campaign-style public relations strategies that reach beyond Washington to Wall Street, Main Street, even Hollywood. In 2003, Merritt took the helm of PCMA and quickly bolstered its stature and clout. He is routinely ranked among the nation’s most effective association executives and is a member of the U.S. Chamber of Commerce’s elite “Committee of 100.” Recognizing his tireless efforts promoting affordable medicines, the Generic Pharmaceutical Association (GPhA) selected Merritt for its 2011“Outstanding Contribution” award. Merritt serves on the Editorial Advisory Board for Drug Benefit News and the Board of The Public Affairs Council, which represents communications professionals worldwide. He holds a BA and MA from Georgetown University. He and his wife Jayne have four children. 24 Speakers Jerry Miller President J. Miller Consulting Jerry Miller, PharmD, is President of J. Miller Consulting, and provides consultative services to pharmaceutical or biotech companies and other healthcare-related firms. He is a former Director of Research with Health Strategies Group, specializing in the PBM and managed markets industry segments. In his twelve years with this firm, he gained recognition as an industry expert by pharmaceutical manufacturer clients and PBM industry senior leaders. Miller has a broad background and experience in multiple areas of the profession of pharmacy including hospital, retail, managed care, Medicaid, and PBMs. His experience includes six years as a member of the pharmacy administrative staff at Cedars-Sinai Medical Center where he supervised the department’s purchasing, emergency, and operating room services, and the Pharmacy & Therapeutics Committee. Joining American Stores in 1988, Miller worked as a Sav-on pharmacy manager, then as the corporate liaison to Cigna of California and Molina Healthcare. He next joined RxAmerica, now owned by CVS Caremark, serving as Director of Clinical Services for over five years. Miller received his Doctor of Pharmacy degree from the University of Southern California in Los Angeles. Betty Nguyen Anchor and Journalist NBC News & MSNBC Betty Nguyen is an award-winning journalist whose work has taken her across the globe. She is an anchor for NBC News & MSNBC and a correspondent for the Today Show. While at the network, Nguyen has covered the Ebola outbreak, the Boston Marathon bombings, the election of Pope Francis, and the birth of Prince George of Cambridge. Before her move to NBC, she was news anchor for CBS This Morning Saturday, a correspondent for The Early Show and anchor for the CBS Morning News. There, she covered the 2012 Presidential election, the death of Osama Bin Laden, the Royal wedding and the Gulf oil spill. Prior to her arrival at CBS, she anchored the weekend edition of CNN Newsroom, where she contributed to CNN’s award-winning coverage of Hurricane Katrina and the tsunami disaster in South Asia. She also traveled to Africa to cover the presidential elections in Sierra Leone, and then to Vietnam to report on deadly flooding in her birth country. Nguyen has interviewed some of the most important newsmakers and celebrities of our time, including the Dalai Lama, President George W. Bush, Sir Richard Branson, Charles Barkley, Lenny Kravitz, Willie Nelson, Dolly Parton, and Usher, just to name a few. In 2015, she was inducted into the Asian Hall of Fame. She is the recipient of a regional Emmy Award and the Legacy of Women Award. In 2007, the Smithsonian Institution recognized Nguyen as the first Vietnamese-American to anchor a national network news program in the United States. Nguyen also spends her time doing humanitarian work. She is the co-founder of Help the Hungry, a non-profit organization that strives to alleviate global hunger by providing humanitarian aid to poverty-stricken families. Her philanthropy work has earned her a spot in the Philanthropy in Texas Hall of Fame. Speakers 25 Kent Rogers Senior Vice President, Industry Relations OptumRx Kent Rogers currently serves as the Senior Vice President, Industry Relations for OptumRx with responsibility for formulary and procurement contracting for all books of business on behalf of internal and external clients of United Health Group. OptumRx is the pharmacy benefit management division of Optum servicing over 66 million members and processing over 1 billion pharmacy claims which represent over $80 billion in drug spend. Rogers has more than 25 years of experience with the pharmaceutical industry, focusing primarily on payer, channel and patient services strategies. Prior to OptumRx, he was a Principal Consultant with Blue Fin Group, served as the Vice President of Managed Markets at Acorda Therapeutics, and held various positions of increasing responsibility within Sales and Managed Markets at Schering Plough and Merck. His career experience includes business development, health economics/outcomes research, building and leading market access teams, developing and implementing payer access and channel strategies, and launching patient services programs. Rogers has a Bachelor of Science in Business Management from Indiana University, and an MBA from Emory University’s Goizueta School of Business. Bill Roth Founding Partner Blue Fin Group Bill Roth is serial entrepreneur and a tenured corporate executive. As Founding Partner of Blue Fin Group, a management consultancy for the pharmaceutical industry, Roth started the company in 2001 and has grown the organization to service most manufacturers and a wide array of channels and service providers. He is considered an innovator and an expert in connecting health care products to patient populations. Roth has consistently forecasted future events in the industry, and he has led his clients and companies to successful outcomes for more than 25 years. Roth has been quoted in dozens of industry publications. He is repeatedly cited by market researchers, analysts, and industry leaders for his accurate predictions, and he speaks frequently at industry events and seminars on the subject of commercialization and related issues. Roth’s unique breadth of experience and knowledge from working with all models in the health care industry provides great context when working to solve challenging business puzzles in our industry. Roth was featured as the cover story of Pharmaceutical Commerce in January 2016 and was featured in Entrepreneur Magazine in 2001. He is also a 2008 recipient of PharmaVOICE magazine’s “Top 100 most-inspiring people in Life Sciences” and was named a 2009 “People to Watch” by PM360 Magazine. 26 Speakers Mike Ryan Senior Vice President, U.S. Value, Access and Policy Bristol-Myers Squibb Dr. Michael L. Ryan, PharmD, is the Senior Vice President for U.S. Value, Access and Policy for Bristol-Myers Squibb. In this role, Ryan is responsible for all pricing, contracting, payer strategy, value and access marketing, and policy across the $8B U.S. BMS portfolio, as well as all field reimbursement strategy, and execution across all U.S. payers. Prior to joining Bristol-Myers Squibb, Ryan spent 16 years at Amgen as the Vice President and General Manager for U.S. Reimbursement, Value and Access, where he was responsible for all pricing, contracting, government price reporting, payer strategy, and value and access marketing across the $13B U.S. Amgen portfolio. He also served as the Vice President and General Manager of the nephrology business unit for Amgen, where he was responsible for the P&L and life cycle management of Amgen’s three products used to treat patients with kidney disease; Epogen®, Aranesp® and Sensipar®. Other roles that Ryan held at Amgen include Vice President and General Manager of Corporate Accounts, where he was responsible for Amgen’s largest corporate customer groups including managed care, integrated health systems, commercial and government payers, group purchasing organizations, pricing, and distribution channels, and he was Senior Director of Central Reimbursement where he was responsible for the analysis and development of legislative and reimbursement strategies across the Amgen portfolio, as well as directing the implementation of such strategies through Amgen’s Government Economics Management sales force. Ryan first joined Amgen in 1999, as Director of Information, Healthcare Economics, and Pharmacy Affairs. Prior to Amgen, Ryan served as Associate Professor and Chairman, Department of Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy, and Executive Director, Department of Pharmacy, and Director, Clinical Information System Implementation, The University of Pittsburgh Medical Center. Ryan also served as President and Executive Director of Community Pharmacy Services Corporation and H.C. Pharmacy, Inc., a University of Pittsburgh Medical Center owned and operated for-profit business and drug wholesaler and distributor. During his tenure at the University of Pittsburgh, Ryan also held affiliated faculty appointments with both the Department of Clinical Pharmacology and the Center for Biomedical Informatics. Ryan is a graduate of the University of California at Los Angeles (1976) and the University of California at San Francisco (1980), and he completed his residency program at the University of Michigan Hospitals and College of Pharmacy in 1981. After completing his residency, Ryan continued to work with the University of Michigan College of Pharmacy and the University of Michigan Medical Center for 15 years. During his career, Ryan has been invited to present over 100 national platform presentations, and he has over 30 refereed journal and textbook publications. The primary focus of Ryan’s research is pharmacoeconomics, pharmacoinformatics, healthcare policy, drug use and disease state management, and the application of Total Quality Management principals to a health care environment. Among his many and varied responsibilities, Ryan has served on numerous national health care committees, directed and/or participated on over 12 Pharmacy and Therapeutics Committees, implemented seven for-profit businesses, developed numerous novel and innovative pharmacy services, directed the implementation of five pharmacy computer systems and the Cerner Millennium Clinical Information System, developed numerous pharmacoinformatic decision support programs, and served as a professor at both the University of Pittsburgh and University of Michigan Schools of Pharmacy and Medical Informatics Training Programs. Speakers 27 George Scangos Chief Executive Officer Biogen George A. Scangos, PhD, is the Chief Executive Officer of Biogen. He has served in this position and as a member of our Board of Directors since July 2010. From 1996 to July 2010, Scangos served as the President and Chief Executive Officer of Exelixis, Inc., a drug discovery and development company, where he continues to serve on the board. From 1993 to 1996, Scangos served as President of Bayer Biotechnology, where he was responsible for research, business development, process development, manufacturing, engineering, and quality assurance of Bayer’s biological products. Before joining Bayer in 1987, Scangos was a professor of biology at Johns Hopkins University for six years, where he is still an adjunct professor. Scangos served as non-executive Chairman of Anadys Pharmaceuticals, Inc., a biopharmaceutical company, from 2005 to July 2010 and was a director of the company from 2003 to July 2010. He also served as the Chair of the California Healthcare Institute in 2010 and was a member of the board of the Global Alliance for TB Drug Development until 2010. Scangos is Chairman of the Board of Directors of Pharmaceutical Research and Manufacturers of America (PhRMA), a member of the Boards of Trustees of the Boston Museum of Science and the Biomedical Science Careers Program, and a member of the National Board of Visitors of the University of California, Davis School of Medicine. Scangos is also on the Board of Directors of Agilent Technologies, Inc., a provider of bioanalytical and electronic measurement solutions. Tim Wentworth President & Chief Executive Officer Express Scripts Tim Wentworth, President and Chief Executive Officer of Express Scripts, is responsible for ensuring Express Scripts delivers on its mission to put medicine within reach of people who need it. Express Scripts is the country’s leading pharmacy benefit manager with 27,000 employees responsible for 1.3 billion annual prescriptions for 3,000 clients and 85 million people. Wentworth joined Express Scripts in 2012 as senior vice president and president, sales and account management. He was promoted to president of the company in 2014, elected to the Board of Directors in January 2015, and became CEO in May 2016. Prior to joining the company, he led the employer and key accounts organizations at Medco Health Solutions for nearly 14 years. In 2006, Wentworth became president and CEO of Accredo specialty pharmacy, leading the rapid and successful integration of Accredo into the broader Medco organization. Before Medco, Wentworth spent five years at Mary Kay, Inc., where he served initially as senior vice president of human resources and subsequently as president, international. He also spent nine years in human resources management at PepsiCo. A well-respected leader in his field, Wentworth has been a featured speaker at Harvard University, the Health Evolution Summit, the American Management Association, and the Best 100 Companies Symposium, among other events. He is a Trustee of the University of Rochester (NY), serving on the Health Strategy and Personnel Committees. Wentworth received his associate’s degree from Monroe Community College and a Bachelor of Science degree in Industrial and Labor Relations from Cornell University. 28 Speakers ABOUT PCMA About PCMA PCMA Board of Directors Chairman, PCMA Board of Directors Vice Chairman and Incoming Chairman Tim Wentworth President & Chief Executive Officer Express Scripts William Fleming Segment Vice President, Humana Inc. President, Humana Pharmacy Solutions Jim DuCharme President & Chief Executive Officer Prime Therapeutics Chris Hocevar President, Select Segment & Cigna Pharmacy Management Cigna Corporation Mark Thierer Chief Executive Officer OptumRx Mostafa Kamal Chief Executive Officer Magellan Rx Management Greg Watanabe President MedImpact Jon Roberts President CVS/caremark & Executive Vice President CVS Health Bill Wolfe Vice President, Pharmacy Aetna PCMA Board of Directors 29 PCMA Staff Mark Merritt President & Chief Executive Officer April Alexander Senior Director, State Affairs Wendy Krasner Vice President, Regulatory Affairs Kristin Bass Senior Vice President, Policy and Federal Affairs Barbara Levy General Counsel Tim Brogan Vice President, Research Greg Lopes Senior Director, Strategic Communications Megan Coder, PharmD Senior Director, Industry Programs Jessica Mazer, Esq Assistant Vice President, State Affairs Andy Cosgrove Vice President, Policy Brian McCarthy Chief Operating Officer Charles Coté Vice President, Strategic Communications Anne McCraw Assistant Vice President, Industry Relations Jenny Dawson Senior Manager, Conferences and Development Casey Murphy Senior Director, Federal Affairs Jonathan Heafitz Assistant Vice President, Federal Affairs Brenda Palmer Chief Financial Officer Ryan Hickey Senior Director, Accounting and Operations Kristen Pumphrey Senior Director, Conferences Greg Johnson Vice President, Strategic Initiatives Meagan Riordan Director, State Affairs Jennifer Joslin Executive Assistant to the President & CEO Deloris Tinsley Executive Assistant Scott Kipper Vice President, State Affairs Scott Woods Senior Director, Policy 30 PCMA Staff PCMA Members PCMA Members 31 2016 PCMA Affiliates 32 2016 PCMA Affiliates MARKETPLACE Marketplace Conference Sponsors PARTN ER S P R E SID EN TIAL SPO N SO R S E X ECU TIVE SPO N SO R S G EN ER AL SPO N SO R S Changing Tomorrow, Together At Astellas, we believe we can make a real impact on the future. That’s why we are fully committed to developing medicines that make a difference where they’re needed most, in areas like oncology, urology, cardiology and transplant. It’s also why we focus on bringing together a diverse group of people with a common goal: to help transform lives. Whether it’s in the office, the laboratory or the community, we’re working together to change tomorrow. @AstellasUS www.astellas.us 080-1021-PM Caring deeply about those around us We know that living with multiple sclerosis (MS) can present some pretty large challenges. At Biogen™, we are committed to patients through ongoing research and support services to help meet unmet needs in the management of MS. Visit Biogen.com, or call 1 800 456 2255. © 2015 Biogen. All rights reserved. 09/15 FCH-US-0947 Otezla® is a registered trademark of Celgene Corporation. © 2016 Celgene Corporation 08/16 USII-APR150131(1)a 44120_ceusps_reminder_ad_resize_fi.indd 1 8/17/16 2:25 PM TURGUT AKMETE Turgut has type 2 diabetes For nearly a century, we have been committed to ending diabetes. And as a leader in research, education, and unique partnerships, we do it for all the patients like Turgut, who never lose hope for a future free from their disease. And that’s why we believe that together we can defeat diabetes in our lifetime. For more about us, visit novonordisk-us.com. © 2012 Novo Nordisk Printed in the U.S.A. 0712-00010441-1 October 2012 We Make Quality Healthcare Accessible Teva Pharmaceuticals is working every day to make quality healthcare accessible around the world. As a manufacturer of specialty and generic pharmaceuticals, Teva provides both new therapies and greater access to quality, affordable medicines. tevausa.com SOLVING THE WORLD’S TOUGHEST HEALTH CHALLENGES TAKES ALL OF US. It takes the will to find a new way forward. And no one gets there alone. That’s why AbbVie teams with peers, academics, clinical experts, and our partners in managed care and specialty pharmacy to take on the most complex health challenges. Uniting the best of pharma with the boldness of biotech, together we’re going beyond conventional thinking to innovate end-to-end approaches that make a real difference. We start with science and work with our colleagues in healthcare to arrive at solutions that help millions of patients live better. abbvie.com BOLD FOR LIFE We are a bold, global pharmaceutical company and a leader in a new industry model – Growth Pharma. Our worldclass team develops, manufactures and commercializes innovative branded pharmaceuticals and biologic products for patients around the world. We are one team of dedicated employees, carving new paths, taking bold, decisive actions to deliver results and better outcomes for patients and providers. www.Allergan.com 78479-R1-V1 What science can do Advancing Quality of Patient Care At AstraZeneca, we know improving the lives of patients requires engagement across all of healthcare, and we are committed to pursuing innovative collaborations that advance quality of care, improve patient outcomes and deliver value to the healthcare system. We also work to support meaningful access to our medicines and actively engage patients in their own care along with their healthcare professionals to help slow progression of disease, reduce readmissions, and decrease complications. To learn more about how AstraZeneca is pushing the boundaries of science to deliver life-changing medicines, transforming serious diseases like cancer, heart disease, diabetes, and asthma, visit astrazeneca-us.com. Oncology combination therapies AstraZeneca is investigating combinations of biologic and small-molecule therapies for the treatment of cancer. These combinations target the tumor directly and some help boost the body’s own immune system to potentially induce cell death. © 2015 AstraZeneca. All rights reserved. 3133005 5/15 At Bayer we encourage you to question the status quo and constantly think beyond the obvious. We foster open discussions, sharing knowledge across our community and partnering with external networks. We always start by listening – because our customers are at the heart of everything we do. At Bayer you have the opportunity to be part of a culture where we value the passion of our employees to innovate and give them the power to change. Passion to innovate | Power to change EB Ad 7.5x10.indd 1 8/18/16 2:46 PM Nurturing innovative ideas today for more health tomorrow. Boehringer Ingelheim ranks among the world’s 20 leading pharmaceutical corporations. Our vision drives us forward. It helps us to foster value through innovation in our company and to look to the future with constantly renewed commitment and ambition. For more than 125 years, Boehringer Ingelheim has been committed to the research and development of innovative medicines that help make more health for patients and their families. Visit us online at us.boehringer-ingelheim.com Imagine what you could build using the nation’s largest electronic prior authorization network. 500+ INTEGRATED EHRs PAYERS REPRESENTING 75% OF U.S. RX VOLUME 600,000+ PROVIDERS NEARLY 48,000 PHARMACIES 80% OF PHARMACY MARKET CoverMyMeds integrates directly into the clinical workflow. covermymeds.com • 1-866-452-5017 access ONCOLOGY SPECIALTY DIGEST PATIENT ADHERENCE PARTNERSHIPS MARKET INSIGHTS NEUROLOGY SECURE DISTRIBUTION PATIENT SUPPORT PROGRAMS PARTNERSHIPS FERTILITY/ ENDOCRINOLOGY NATIONAL/LOCAL SUPPORT ©2016 EMD Serono, Inc. US-MLT-0316-0002 We believe in more than the big breakthroughs. And more than the next big thing. We believe in the day-in day-out work of making science happen. And the millions of little victories — and failures — in between the breakthroughs. Because to us, it’s the daily effort of everyday people that changes the future. So we don’t stop. We keep working. Every day. Jacki, patient Advancing Therapeutics, Improving Lives. For more than 25 years, Gilead has worked to develop medicines that address areas of unmet medical need for people around the world. Our portfolio of medicines and pipeline of investigational drugs include treatments for HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions. Every day we strive to transform and simplify care for people with life-threatening illnesses. For more information, please visit www.gilead.com. © 2015 Gilead Sciences, Inc. But in order to fully achieve our mission of helping people do more, feel better and live longer, we need to go beyond discovering, developing and delivering new medicines, vaccines and healthcare products. That’s why we support innovative health and education programs designed to bring sustainable, positive change in local communities across America. © 2001– 2016 GLAXOSMITHKLINE ALL RIGHTS RESERVED. Every challenge creates opportunity Every relationship brings responsibility Providing services for Janssen Pharmaceutical Companies of Johnson & Johnson Every patient is our inspiration © Johnson & Johnson Health Care Systems Inc. 2015 February 2015 027922-150115 Hong Hu, Research Advisor, Lilly Research Laboratories It begins with a promise to discover medicines that make life better. Since 1876, we have worked tirelessly to develop and deliver trusted medicines that meet real needs, finding ways to come through no matter the odds. From the development of insulin to the discovery of new treatments for mental illness, we have pioneered breakthroughs against some of the most stubborn and devastating diseases. We bring this same determination to our work today, uniting our expertise with the creativity of research partners across the globe to keep finding ways to make life better. To find out more about our promise, visit www.lilly.com/about. 2016 CA Approved for External Use PRINTED IN USA ©2016, Eli Lilly and Company. ALL RIGHTS RESERVED. Navigating the path to medication access Novartis Oncology is committed to helping patients living with cancer receive the medicines they need. Patient Assistance Now Oncology (PANO) offers quick and easy access to information about our wide range of resources. SUPPORT FOR PATIENTS INCLUDES: • Support with insurance verification • Medicare education • Alternative assistance searches and referrals to federal or state assistance programs • Support for Novartis Oncology medication • Patients prequalified via phone screening for the Patient Assistance Program (PAP) will be sent a 30-day supply of their needed medication while completing the application • Information about financial or co-pay assistance that may be available via independent charitable foundations GET ACCESS NOW Visit www.OncologyAccessNow.com/patient, or call 1-800-282-7630, to speak with a member of our knowledgeable staff dedicated to making access to therapy as simple and convenient as possible. Novartis Pharmaceuticals Corporation East Hanover, New Jersey 07936-1080 © 2015 Novartis 10/15 T-PAN-1125452 18,000 More than employees in the United States A comprehensive offering of medicines, vaccines and innovative services all over the world 120 © Blue Images/Corbis - ooyoo/getty images More than locations across North America SANOFI FOCUSED ON PATIENTS’NEEDS Over the years, Sanofi has evolved to meet the new challenges of healthcare worldwide. Today, Sanofi is a global healthcare leader focused on patients. We listen to their needs, treat them, and provide support to them. Through our diversified portfolio of medicines, vaccines and innovative therapeutic solutions, we strive to protect the health and meet the needs of the world’s 7 billion people. US.COR.14.06.005 For more information: www.sanofi.com – www.sanofi.us www.facebook.com/sanofiUS www.twitter.com/sanofiUS www.pinterest.com/sanofiUS blog.sanofi.us T:7.5” T:10” UNMET NEEDS REQUIRE UNMATCHED COMMITMENT. The combined talents and energy of Shire and Baxalta are uniting in common cause: to make a difference in the lives of those living with and affected by rare diseases and highly specialized conditions. For more information, please visit shire.com INTSP/C-ANPROM/CORP/16/0022 S13862 05/16 Sunovion supports PCMA in its mission to promote industry relations and thought leadership throughout the pharmaceutical supply chain A proud sponsor of the 2016 PCMA Annual Meeting, Sunovion is a global biopharmaceutical company focused on the innovative application of science and medicine to help people with serious medical conditions. Our spirit of innovation is driven by the conviction that scientific excellence paired with meaningful advocacy and relevant education can improve lives. Visit us at www.sunovion.com and connect with us on Twitter @Sunovion and LinkedIn. Working in Partnership with You We’re driven to improve people’s lives. Takeda strives toward better health for people worldwide through leading innovation in medicine. At Takeda, we make a commitment to make a difference. Takeda Pharmaceuticals U.S.A., Inc. www.takeda.us USD/TAK/15/0042i THE SCIENCE of POSSIBILITY Vertex creates new possibilities in medicine to cure diseases and improve people’s lives. We work with leading researchers, doctors, public health experts and other collaborators who share our vision for transforming the lives of people with serious diseases, their families and society. www.vrtx.com © 2016 Vertex Pharmaceuticals Incorporated CONTINUING OUR COMMITMENT TO PAH Actelion Pharmaceuticals is proud to support the Pulmonary Hypertension Association in advancing the treatment and care of patients with PAH. © 2015 Actelion Pharmaceuticals US, Inc. All rights reserved. ACT-00747 0315 FOCUSED ON DEVELOPING SPECIALTY TREATMENTS for debilitating diseases that are often difficult to diagnose and treat, providing hope to patients and their families. www.sanofigenzyme.com Lundbeck is a pharmaceutical company committed to improving the lives of those suffering from psychiatric and neurological disorders. We support and participate in hundreds of community awareness and educational events each year. This participation fuels our passion to make a difference, one patient at a time. To learn more about Lundbeck, visit www.lundbeckus.com. UBR-D-00077 SEEING COMPLEXITY IN A NEW LIGHT. For nearly 150 years, Mallinckrodt has made complex scientific problems manageable, developing valuable treatments and diagnostic tools for patients who need them. Learn more at Mallinckrodt.com Mallinckrodt, the “M” brand mark and the Mallinckrodt Pharmaceuticals logo are trademarks of a Mallinckrodt company. © 2016 Mallinckrodt. July 2016 Welcome to Scottsdale, elevation 1,150 to 4,877 feet At Medivation, we strive to transform and elevate patients’ lives with our medically innovative therapies To ensure patients have access to our medical solutions, we partner with a network of specialty pharmacies and provide educational resources with every prescription delivery. Contact a National Account Director for more information or visit medivation.com. A proud supporter of the PCMA ©2016 rights reserved. reserved. Printed Printed in in USA. USA. XXX-XXX-XX-XXXX CCM-MDV-US-0023 7/16 ©2016 Medivation, Medivation, Inc. Inc. All All rights 12/15 MEDICAL BREAKTHROUGHS MAY COME OUT OF THE LAB. BUT THEY BEGIN IN THE HEART. For more than 150 years, a very special passion has driven the people of Merck. Our goal is to develop medicines, vaccines, consumer care and animal health innovations that will improve the lives of millions. Still, we know there is much more to be done. And we’re doing it, with a long-standing commitment to research and development. We’re just as committed to expanding access to healthcare and working with others who share our passion to create a healthier world. Together, we’ll meet that challenge. With all our heart. For more information about getting Merck medicines and vaccines for free, visit merckhelps.com or call 800-727-5400. Copyright © 2013 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. All Rights Reserved. CORP-1060080-0006 01/13 MerckAd_Lab_Half_Clr.indd 1 2/5/13 10:24 AM Mylan believes we all share one wish – to go where our dreams take us. At Mylan, we’re committed to helping people live their dreams by providing access to high quality medicine for the world’s 7 billion people, one person at a time. Mylan.com August 2016 01US16EUC0093 The development of opioids formulated to deter abuse is a high public health priority.1 Visit TeamAgainstOpioidAbuse.com Reference: 1. Food and Drug Administration, Center for Drug Evaluation and Research (CDER), US Department of Health and Human Services. Abuse-Deterrent Opioids — Evaluation and Labeling: Guidance for Industry. April 2015. http://www.fda.gov/downloads/ drugs/guidancecomplianceregulatoryinformation/guidances/ucm334743.pdf. Accessed August 17, 2016. ©2016 Purdue Pharma L.P., Stamford, CT 06901-3431 MR-02050 B10211-PCMA 8/16 Valeant Pharmaceuticals International, Inc. is committed to innovation and to improving people’s lives through its healthcare products. W W W.VA L E A N T.C OM Acorda’s mission is to develop therapies that restore function and improve the lives of people with neurological disorders. We are proud to be a sponsor of the Pharmaceutical Care Management Association’s Annual Meeting. www.acorda.com The stylized Acorda logo is a trademark of Acorda Therapeutics, Inc. © 2015 Acorda Therapeutics, Inc. All rights reserved. 8/15 MS3735 We Understand Your Challenges. We Are Committed to Seeking Solutions. We are dedicated to developing therapies and navigating treatment management challenges to help payers, providers and patients address the burden of CNS diseases. A global biopharmaceutical company with fully integrated R&D, manufacturing and commercial capabilities in the U.S. For more information, reach out to your Alkermes Account Director or visit us at www.alkermes.com ©2016 Alkermes. All Rights Reserved. OT-001345 At Bristol-Myers Squibb, we are working together for patients. Our mission is clear — we discover, develop and deliver transformational medicines that help people prevail over serious diseases. Our sense of urgency is real — we work every day to push the boundaries of scientific discovery and to make a meaningful difference in the lives of patients. It’s what we do. It’s why we do it. www.bms.com © 2016 Bristol-Myers Squibb Company Ingenuity in Medicine Visit collegiumpharma.com for more information © 2016 Collegium Pharmaceutical, Inc. All rights reserved. PP-CORP-US-0016 8/16 1607066_PCMA-Ad-082516-v5.indd 1 8/26/16 1:46 PM Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical products to address diversified, unmet medical needs of patients in both mature and emerging markets. With over 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for hypertension and thrombotic disorders, under the Group’s 2025 Vision to become a “Global Pharma Innovator with a Competitive Advantage in Oncology,” Daiichi Sankyo research and development is primarily focused on bringing forth novel therapies in oncology, including immuno-oncology, with additional focus on new horizon areas, such as pain management, neurodegenerative diseases, heart and kidney diseases, and other rare diseases. For more information, please visit: www.daiichisankyo.com. Daiichi Sankyo, Inc., headquartered in Parsippany, New Jersey, is a member of the Daiichi Sankyo Group. To learn more about Daiichi Sankyo, Inc., visit www.dsi.com. DSNA16102716 Half-page-no-bleed-horizontal-color-b.indd 6 08/16 8/11/16 3:26 PM Introducing the World’s First Continuous Glucose Monitoring (CGM) System on the Phone See glucose in a whole new way with Dexcom G5® Mobile CGM System* CGM reveals what no meter can. Unlike fingersticks that give a number for a single point in time, CGM lets you see your glucose in real time so you’ll always know when your glucose is trending high, low or when you’re good to go.** With Dexcom G5 Mobile CGM System, viewing your data is easier than ever. With glucose information displayed directly onto your smart phone,*** you’ll get the ultimate in convenience and discretion. Always know with Dexcom G5 Mobile CGM System. To learn more, visit dexcom.com/G5Mobile. BRIEF SAFETY STATEMENT The Dexcom G5 Mobile Continuous Glucose Monitoring System (the “System”) is a glucose monitoring system indicated for detecting trends and tracking patterns in persons (age 2 years and older) with diabetes. CONTRAINDICATIONS Remove the System (sensor, transmitter, and receiver) before Magnetic Resonance Imaging (MRI), Computed Tomography (CT) scan, or high-frequency electrical heat (diathermy) treatment. The System is MR Unsafe. Do not bring any portion of the System into the MR environment. Taking acetaminophen while wearing the sensor may falsely raise your sensor glucose readings. WARNING Do not use the System for treatment decisions. The System does not replace a blood glucose meter. The System is not approved for use in pregnant women, persons on dialysis or critically ill persons. If a sensor breaks and no portion of it is visible above the skin, do not attempt to remove it. Seek professional medical help if you have infection or inflammation. Report broken sensors to Dexcom Technical Support. Sensor placement is not approved for sites other than under the skin of the belly (ages 2 years and older) or upper buttocks (ages 2-17 years). Your smart device’s internal settings override your Dexcom app settings. Accessory devices (like a smart watch) might override your smart device’s alert and notification settings. The Share feature must be turned “On” with an active internet connection to communicate glucose information to a Follower. The Follower must download and install the Dexcom Follow App onto a separate smart device with an active internet connection to receive data. Contact Dexcom Toll Free at 877-339-2664 or www.dexcom.com for detailed indications for use and safety information. * Dexcom G5 Mobile Continuous Glucose Monitoring System, User’s Guide, 2015. ** The Dexcom G5 Mobile CGM System does not replace a blood glucose meter. Always use the values from your blood glucose meter for treatment decisions. *** To view a list of compatible devices, visit www.dexcom.com/compatibility LBL013625 Rev002 ©2016 Dexcom Inc. All rights reserved. Passionate about patient care Eisai’s passionate commitment to patient care is the driving force behind our efforts to find innovative solutions that help address unmet medical needs and contribute to the wellbeing of patients worldwide. With therapies in oncology and specialty care, we focus on having an impact on patients and their families. At Eisai, human health care is our goal. CORP-US0023 ©2016 Eisai Inc. All rights reserved. Aug 2015 www.eisai.com/us Improving Lives,Creating Value. TM At Endo International, our specialty branded pharmaceuticals, generic products and over-the-counter medications play an important role in helping millions of patients lead healthier lives. Through our operating companies, we are dedicated to serving our patients, customers and shareholders as we continually search for new and better ways to do things while creating value. www.endo.com © 2016 Endo. All Rights Reserved. Help your new-to-dialysis patients succeed with Velphoro Start with high potency. Stay with long-term control.* 1 Long-term efficacy with a low pill burden†1,2 Long-term tolerability as demonstrated in the 52-week study†1,2 Access and affordability for most patients VISIT VELPHORO.COM/HCP TO DOWNLOAD $0 CO-PAY SAVINGS CARDS AND OTHER RESOURCES. *Clinical results of individual patients from long-term trial. INDICATION Velphoro® (sucroferric oxyhydroxide) is a phosphate binder indicated for the control of serum phosphorus levels in patients with chronic kidney disease on dialysis. IMPORTANT SAFETY INFORMATION • Velphoro must be administered with meals. Velphoro tablets must be chewed and not swallowed whole. To aid with chewing and swallowing, the tablets may be crushed. • Patients with peritonitis during peritoneal dialysis, significant gastric or hepatic disorders, following major gastrointestinal (GI) surgery, or with a history of hemochromatosis or other diseases with iron accumulation have not been included in clinical studies with Velphoro. Monitor effect and iron homeostasis in such patients. • In a parallel design, fixed-dose study of 6 weeks duration, the most common adverse drug reactions to Velphoro chewable tablets in hemodialysis patients included discolored feces (12%) and diarrhea (6%). • Velphoro can be administered concomitantly with oral calcitriol, ciprofloxacin, digoxin, enalapril, furosemide, HMG CoA reductase inhibitors, hydrochlorothiazide, losartan, metoprolol, nifedipine, omeprazole, quinidine and warfarin. Take doxycycline at least 1 hour before Velphoro. Velphoro should not be prescribed with oral levothyroxine. Please see Brief Summary on adjacent page or visit www.Velphoro.com for full Prescribing Information. A 52-week, open-label, active-controlled, phase 3 study evaluated the safety and efficacy of Velphoro in lowering serum phosphorus levels in patients (N=1,054) with chronic kidney disease on hemodialysis or peritoneal dialysis.1 † References: 1. Velphoro® [package insert]. Waltham, MA: Fresenius Medical Care North America; 2014. 2. Floege J, Covic AC, Ketteler M, et al; on behalf of the Sucroferric Oxyhydroxide Study Group. Long-term effects of the iron-based phosphate binder, sucroferric oxyhydroxide, in dialysis patients. Nephrol Dial Transplant. 2015;30(6):1037-1046. Velphoro is a registered trademark of Vifor Fresenius Medical Care Renal Pharma Ltd. Distributed by: Fresenius Medical Care North America Waltham, MA 02451 © 2016 Fresenius Medical Care, all rights reserved. PN 102983-01 Rev. A 03/2016 Brief Summary: Please see Full Prescribing Information for additional information seen in animal studies with doses up to 16 times the maximum recommended clinical dose on a body weight basis. The effects of Velphoro on labor and delivery in humans are not known. Nursing Mothers Since the absorption of iron from Velphoro is minimal, excretion of Velphoro in breast milk is unlikely. INDICATIONS AND USAGE Velphoro (sucroferric oxyhydroxide) is a phosphate binder indicated for the control of serum phosphorus levels in patients with chronic kidney disease on dialysis. DOSAGE AND ADMINISTRATION Velphoro tablets must be chewed and not swallowed whole. To aid with chewing and swallowing, tablets may be crushed. The recommended starting dose of Velphoro is 3 tablets (1,500 mg) per day, administered as 1 tablet (500 mg) 3 times daily with meals. Adjust by 1 tablet per day as needed until an acceptable serum phosphorus level is reached, with regular monitoring afterwards. Titrate as often as weekly. DOSAGE FORMS AND STRENGTHS Velphoro (sucroferric oxyhydroxide) chewable tablet 500 mg. CONTRAINDICATIONS None. WARNINGS AND PRECAUTIONS Pediatric Use The safety and efficacy of Velphoro have not been established in pediatric patients. Geriatric Use Of the total number of subjects in two active-controlled clinical studies of Velphoro (N=835), 29.7% (n=248) were 65 and over. No overall differences in safety or effectiveness were observed between these subjects and younger subjects. OVERDOSAGE There are no reports of overdosage with Velphoro in patients. Since the absorption of iron from Velphoro is low, the risk of systemic iron toxicity is low. Hypophosphatemia should be treated by standard clinical practice. Velphoro has been studied in doses up to 3,000 mg per day. HOW SUPPLIED/STORAGE AND HANDLING Velphoro are chewable tablets supplied as brown, circular, bi-planar tablets, embossed with “PA 500” on 1 side. Each tablet of Velphoro contains 500 mg iron as sucroferric oxyhydroxide. Velphoro tablets are packaged as follows: NDC 49230-645-51 Bottle of 90 chewable tablets Patients with peritonitis during peritoneal dialysis, significant gastric or hepatic disorders, following major gastrointestinal surgery, or with a history of hemochromatosis or other diseases with iron accumulation have not been included in clinical studies with Velphoro. Monitor effect and iron homeostasis in such patients. Storage Store in the original package and keep the bottle tightly closed in order to protect from moisture. Store at 25°C (77°F) with excursions permitted to 15 to 30°C (59 to 86°F). ADVERSE REACTIONS PATIENT COUNSELING INFORMATION In a parallel design, fixed-dose study of 6 weeks duration, the most common adverse drug reactions to Velphoro chewable tablets in hemodialysis patients included discolored feces (12%) and diarrhea (6%). To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Medical Care North America at 1-800-323-5188 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. DRUG INTERACTIONS Velphoro can be administered concomitantly with oral calcitriol, ciprofloxacin, digoxin, enalapril, furosemide, HMG-CoA reductase inhibitors, hydrochlorothiazide, losartan, metoprolol, nifedipine, omeprazole, quinidine and warfarin. Take doxycycline at least 1 hour before Velphoro. Velphoro should not be prescribed with oral levothyroxine. USE IN SPECIFIC POPULATIONS Pregnancy Pregnancy Category B: Reproduction studies have been performed in rats and rabbits at doses up to 16 and 4 times, respectively, the human maximum recommended clinical dose on a body weight basis, and have not revealed evidence of impaired fertility or harm to the fetus due to Velphoro. However, Velphoro at a dose up to 16 times the maximum clinical dose was associated with an increase in post-implantation loss in pregnant rats. Animal reproduction studies are not always predictive of human response. There are no adequate and well-controlled studies in pregnant women. Labor and Delivery No Velphoro treatment-related effects on labor and delivery were Inform patients that Velphoro tablets must be chewed and not swallowed whole. To aid with chewing and swallowing, the tablets may be crushed [see Dosage and Administration]. Velphoro should be taken with meals. Instruct patients on concomitant medications that should be dosed apart from Velphoro [see Drug Interactions]. Inform patients that Velphoro can cause discolored (black) stool. Distributed by: Fresenius Medical Care North America 920 Winter Street Waltham, MA 02451 US Patent Nos. 6174442 and pending, comparable and/or related patents. © 2014 Fresenius Medical Care North America. All rights reserved. MORE THAN 75 YEARS OF IMPROVING THE HEALTH & WELL-BEING OF PEOPLE WORLDWIDE At Grifols, we are proud of our pioneering spirit and history of innovation. In 1940, we founded a company that has helped transform hematology. Learn more about Grifols at www.grifols.com Ad_PCMA_16.indd 1 US/CO/0116/0049 Today, we are a global leader providing life-saving protein therapies, diagnostic solutions, and other tools that hospitals, pharmacies, and healthcare professionals need to deliver expert medical care. 14/7/16 8:23 Trim: 7.5” Live: 7” A legacy of trust. A future of care. © Kowa Pharmaceuticals America, Inc. (2016) All rights reserved. GEN-1214 August 2016 Trim: 4.75” Live: 4.25” Kowa Pharmaceuticals is committed to developing and delivering safe, effective solutions in the field of cardiometabolic therapeutics. We do this by maintaining high ethical and professional standards—and it all starts with people. By empowering our employees to live this mission, we can create a healthier vision for the future. Science drives our business, and passion drives our science. At Regeneron, we bring innovative thinking to the discovery, development and commercialization of treatments that help improve the lives of patients in need. IMPROVING PATIENT ACCESS Upsher-Smith Laboratories, Inc. is committed to providing healthcare solutions that aim to deliver better outcomes and enhance life. In pursuit of that mission, we’re dedicated to partnering with managed care organizations to improve patients’ access to medications they need. What sets us apart from our competitors is our long track record of strong relationships and reliable service. We work hard to offer quality, affordable medications, ranging from generics to central nervous system (CNS) products, which we strive to keep in consistent supply. And we can always be counted on to sell our products at prices that deliver good value. It is our belief that when time and money are saved, everyone benefits — especially patients. Learn more by contacting our managed care team at 1-800-654-2299. Upsher-Smith Laboratories, Inc., 6701 Evenstad Drive, Maple Grove, MN 55369 © 2016 Upsher-Smith Laboratories, Inc. 110767.02 1-800-654-2299 Established 1999 Please join us in thanking the following sponsors for their support of this year’s Annual Meeting. PARTN ER S P R E SID EN TIAL SPO N SO R S E X ECU TIVE SPO N SO R S G EN ER AL SPO N SO R S Join us next year sPCMA Business Forum 2017 PCMA Annual Meeting 2017 March 8 & 9 September 25 & 26 Hilton Bonnet Creek Orlando, FL The Westin Kierland Scottsdale, AZ pcmanet.org
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