Print Form New York University Hazardous Material Shipping Declaration (Please Print) Your name: Date (MM/DD/YYYY): HAZARDOUS MATERIAL GENERAL INFORMATION Material Name: Form of Material: □ solid □ liquid □ gas Type of Material? □ chemical □ radiological □ biological Quantity of Material: CAS Number: (if any) Manufacturer: (if any) Shipping Destination: Special Shipping Requirements: (i.e., cold packs, dry ice) Preferred Shipping Method: (i.e. US Mail, Fed Ex, UPS) CHEMICAL INFORMATION Percent concentration: Other information: RADIOLOGICAL INFORMATION Radionuclide: Activity: Other information: BIOLOGICAL INFORMATION GENETICALLY MODIFIED ORGANISMS □ Genetically modified microorganisms and organisms that are not infectious to humans or animals (i.e., are WHO Risk Group 1) and do not interact in a way that could alter animals, plants, or microbiological substances in a way which is not normally the result of natural reproduction. □ Genetically modified microorganisms and organisms that are not infectious (i.e., are Risk Group 1) but which are capable of altering animals, plants or microbiological substances in a way which is not normally the result of natural reproduction. □ Genetically modified microorganisms and organisms that meet the definition of infectious substances for humans (i.e., WHO Risk Groups 2-4) □ Genetically modified microorganisms and organisms that meet the definition of infectious substances for animals only (i.e., WHO Risk Groups 2-4) Microorganisms (bacteria, mycoplasms, viruses, fungi, etc.) □ Microorganisms that are not infectious to humans or animals (i.e., are WHO Risk Group 1) □ Microorganisms that meet the definition of infectious substances for humans (i.e., who Risk Groups 2-4) □ Microorganisms that meet the definition of infectious substances for animals only (i.e., who Risk Groups 2-4) □ Biological products containing pathogens in Risk Group 1; and those known NOT to contain pathogens in Risk Groups 2-4. □ Biological products, including an experimental product or component of a product, subject to Federal (e.g., the FDA, or USDA) approval, permit, or licensing requirements. □ Biological products reasonably expected to contain pathogens in Risk Groups 2-4 that do not meet the requirements of the trade exemption above AND meet the definition of infectious substances for humans. □ Biological products reasonably expected to contain pathogens in Risk Groups 2-4 that do not meet the requirements of the trade exemption above AND meet the definition of infectious substances for animals only. □ Patient specimens are those collected directly from humans or animals for purposes such as research, diagnosis, investigational activities, disease treatment and prevention: □ specimen known to contain or suspected to contain a microorganism in Risk Group 1, or that does not contain a pathogen, or one in which the pathogen has been neutralized or inactivated. □ specimen with no known serious human or animal disease. [E.g. Tumors & clinical samples received by Cell Genesys] □ Blood, blood products, and organs for donation. □ specimen with known serious human or animal disease (Risk Group 4). WARNING: Failure to comply in all respects with the applicable Dangerous Goods Regulations may be in breach of the applicable law, subject to legal penalties. * This Declaration must be signed by the principal investigator or it will not be processed. CERTIFICATION: I hereby declare that the contents of this consignment are fully and accurately described above. Print name and title of signatory: Campus address and phone: P.I. Signature: * Date:
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