China Lifts Drug Price Controls But Heightens

MAY 14, 2015
GLOBAL LIFE SCIENCES: CHINA UPDATE
China Lifts Drug Price Controls But Heightens Drug Price
Monitoring and Enforcement
On May 4, 2015, seven Chinese government agencies jointly announced that they will lift price controls for most
drug products, and establish a market-oriented drug pricing mechanism. This will have a fundamental impact on
the pricing mechanisms of drug companies in China. On the same day, the National Development and Reform
Commission (NDRC) announced that it will increase its monitoring of illegal pricing behaviors and launch an
enforcement campaign, and this will significantly heighten the risks that companies will face in case of violation.
The joint announcement by the seven government agencies, titled the Opinion on Advancing the Drug Price
Reform, manifests that the goal of the reform is to “establish a market-oriented drug pricing mechanism, and
reduce to the maximum extent the government’s direct interference with drug pricing.” Specifically, the
following changes will be implemented from June 1, 2015:
•
For patented drugs and drugs manufactured by one company only, the government will establish a price
negotiation mechanism participated by stakeholders of the healthcare system, such as pharmaceutical
companies, hospitals, and provincial governments.
•
For drugs covered by government insurance programs, the government will formulate the standards for
government payment for drugs.
•
For blood products not covered by medical insurance, vaccines covered by national procurement programs,
AIDS drugs paid by the government, and contraceptive drugs and devices, prices will be determined through
drug bidding programs or negotiation.
•
For narcotic drugs and psychotropic drugs, Maximum Ex-Works Prices and Maximum Retail Prices will be
maintained.
•
For all other drugs, Maximum Ex-Works Prices and Maximum Retail Prices will be lifted, and the
manufacturers are allowed to decide drug prices on their own.
Sidley Austin provides this information as a service to clients and other friends for educational purposes only. It should not be construed or relied on as legal advice or to create a
lawyer-client relationship. Attorney Advertising - For purposes of compliance with New York State Bar rules, our headquarters are Sidley Austin LLP, 787 Seventh Avenue, New York,
NY 10019, 212.839.5300; One South Dearborn, Chicago, IL 60603, 312.853.7000; and 1501 K Street, N.W., Washington, D.C. 20005, 202.736.8000.
NAME OF UPDATE
Page 2
The Opinion also lays out drug price monitoring measures after the drug price control is lifted. NDRC issued a
companion document, the Notice on Strengthening Monitoring of Drug Prices, to detail the drug price
monitoring measures. These include:
•
The government will monitor the Ex-Works Prices or landed prices of “drugs with insufficient competition.”
•
The government will monitor drugs that present the following drug irregularities, and may conduct
investigations when necessary: (i) frequent or significant drug price fluctuations; (ii) significant price
differences with drugs in other countries, or other drugs of the same type, or drugs in other regions in China.
•
Specifically, the government will focus its investigation on companies selling drugs at unreasonably high
prices by abusing market dominant positions.
•
NDRC announced that it will start a half-year drug price inspection program. If a drug company engages in
serious violations, NDRC will make a recommendation to health authorities to ban this company from drug
procurement programs for two years.
After lifting its direct drug price control, the Chinese Government will shift its focus of drug price administration
to monitoring of drug pricing violations and increase its enforcement in this area. Therefore, multinational drug
companies, in addition to necessary business adjustments, should revisit their price compliance programs,
including antitrust compliance programs, to ensure there is no violation of government pricing regulations,
particularly relevant provisions in antitrust laws.
05-14-2015-Global-Life-Sciences-China-Update
If you have any questions regarding this Sidley Update, please contact the Sidley lawyer with whom you usually work, or
Chen Yang
Partner
+86.10.5905.5600
[email protected]
Lei Li
Partner
+86.10.5905.5505
[email protected]
NAME OF UPDATE
Page 3
Sidley China Life Sciences Practice
Sidley has a powerful, fully integrated life sciences practice serving multi-national pharmaceutical, biotechnology, medical device
and food companies in every aspect of their business operations in China. Sidley’s Foreign Direct Investment, general Commercial,
Corporate, M&A/Joint Venture, Antitrust, FCPA, Licensing, IP, and provincial government work, as well our Regulatory practice
permits us to serve virtually every legal need of our life sciences clients in China.
Sidley is the first international law firm to establish a stand-alone, comprehensive food and drug regulatory practice in China. As an
integral part of our Global Life Sciences practice, we bring our knowledge of industry practices in the U.S. and EU to each project in
China and help develop global Standard Operation Procedures (SOPs) and benchmark best practices.
For further information on the China Life Sciences Practice, please contact:
Chen Yang
Zhengyu Tang
Yuet Ming Tham
Joseph Chan
Partner
Partner
Partner
Partner
+86.10.5905.5600
+86.21.2322.9318
+852.2509.7645
+86.21.2322.9328
[email protected]
[email protected]
[email protected]
[email protected]
Lei Li
Wenseng “Wendy” Pan
Partner
+1.212.839.8544
+86.10.5905.5505
[email protected]
[email protected]
Sidley Global Life Sciences Practice
On three continents, Sidley’s Global Life Sciences Practice team offers coordinated cross-border and national advice on Food, Drug
and Medical Device Regulatory, Life Sciences Enforcement, Litigation and Compliance, Healthcare Regulatory, Products Liability,
Intellectual Property, Corporate and Technology Transactions, Securities and Corporate Finance, International Trade and
Arbitration, FCPA/Anti-Corruption, Antitrust/Competition, and Environmental/Nanotechnology.
Globally rated as one of the top life sciences practices, our team includes former senior government officials, medical doctors and
leaders in various life sciences fields.
For further information on the Global Life Sciences Practice, please contact:
Scott Bass
James C. Stansel
Paul E. Kalb, M.D.
+1.202.736.8684
+1.202.736.8092
+1.202.736.8050
+1.212.839.5613
[email protected]
[email protected]
[email protected]
M. Patricia Thayer
David J. Zampa
+1.415.772.7469
+1.312.853.4573
+1.650.565.7569
[email protected]
[email protected]
To receive Sidley Updates, please subscribe at www.sidley.com/subscribe.
BEIJING · BOSTON · BRUSSELS · CHICAGO · DALLAS · GENEVA · HONG KONG · HOUSTON · LONDON · LOS ANGELES NEW YORK ·
PALO ALTO · SAN FRANCISCO · SHANGHAI · SINGAPORE · SYDNEY · TOKYO · WASHINGTON, D.C.
Sidley Austin refers to Sidley Austin LLP and affiliated partnerships as explained at www.sidley.com/disclaimer.
www.sidley.com or www.sidley.com.cn