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Biological Material Transfer Agreement
"I need a Biological Material Transfer Agreement for transferring cell lines from our university research lab to a pharmaceutical company for cancer research, with strict confidentiality provisions and publication rights for our researchers."
1. Parties: Identification of the Provider and Recipient institutions and their authorized representatives
2. Background: Context of the transfer, relationship between parties, and purpose of the agreement
3. Definitions: Detailed definitions of key terms including 'Material', 'Progeny', 'Unmodified Derivatives', 'Modifications', and 'Commercial Purposes'
4. Material Transfer: Details of the biological materials being transferred, including quantity, form, and shipping arrangements
5. Use of Material: Permitted uses, restrictions, and scope of authorized research
6. Compliance: Requirements for regulatory compliance, biosafety, and handling procedures
7. Intellectual Property: Rights to materials, derivatives, and research results
8. Confidentiality: Obligations regarding confidential information related to the materials
9. Publication: Rights and requirements for publishing research results
10. Warranties and Liability: Disclaimers, warranties, and allocation of risks
11. Term and Termination: Duration of agreement, termination conditions, and post-termination obligations
12. General Provisions: Standard clauses including notices, assignment, governing law, and entire agreement
1. Commercial Use: Required when there is potential for commercial exploitation of research results
2. Human Biological Materials: Additional provisions required when transferring human specimens or derivatives
3. Export Control: Required for international transfers or materials subject to export restrictions
4. Cost Recovery: Include when the provider charges fees for material preparation and shipping
5. Third Party Rights: Required when materials incorporate third-party components or rights
6. Data Protection: Required when personal data is associated with biological materials
7. Return or Destruction: Specific requirements for material disposition after project completion
1. Schedule A - Material Description: Detailed technical description of the biological materials, including source, characterization, and quantity
2. Schedule B - Research Plan: Description of the intended research, methodology, and objectives
3. Schedule C - Biosafety Requirements: Specific handling, containment, and safety procedures required for the materials
4. Schedule D - Fee Schedule: Breakdown of any applicable fees for material preparation and transfer
5. Schedule E - Contact Information: Detailed contact information for key personnel and authorized representatives
6. Appendix 1 - Shipping Instructions: Detailed protocols for packaging, labeling, and shipping the materials
7. Appendix 2 - Required Permits: Copies or details of required permits, certifications, or authorizations
Authors
Biotechnology
Healthcare
Pharmaceuticals
Academic Research
Medical Research
Agriculture
Environmental Science
Clinical Research
Life Sciences
Public Health
Legal
Research and Development
Regulatory Affairs
Technology Transfer Office
Laboratory Operations
Quality Assurance
Research Administration
Compliance
Intellectual Property
Scientific Operations
Research Director
Laboratory Manager
Principal Investigator
Technology Transfer Officer
Legal Counsel
Biosafety Officer
Research Compliance Manager
Scientific Director
Intellectual Property Manager
Research Administrator
Quality Assurance Manager
Regulatory Affairs Specialist
Contract Manager
Research Scientist
Laboratory Supervisor
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