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1. Commercial Use Provisions: Required when there is potential for commercial exploitation of research results

2. Benefit Sharing: Needed when the material originates from indigenous resources or involves traditional knowledge

3. Export Control Compliance: Required for international transfers of controlled biological materials

4. Biosafety Requirements: Necessary for hazardous or genetically modified materials

5. Data Protection: Required when personal data or sensitive genetic information is involved

6. Traditional Knowledge Rights: Needed when the material involves indigenous or traditional knowledge

7. Third Party Rights: Required when the material or its use involves third party intellectual property

8. Material Tracking Requirements: Necessary for materials requiring special monitoring or reporting

1. Schedule A - Material Description: Detailed technical description of the biological material, including origin, characteristics, and quantity

2. Schedule B - Transfer Protocols: Specific procedures for packaging, shipping, and handling of the material

3. Schedule C - Safety Data Sheet: Safety information and handling requirements for hazardous materials

4. Schedule D - Research Plan: Detailed description of the intended research and experimental procedures

5. Schedule E - Fee Schedule: Details of any transfer fees, maintenance costs, or other financial terms

6. Appendix 1 - Compliance Certificates: Copies of relevant regulatory approvals and permits

7. Appendix 2 - Contact Information: List of authorized personnel and emergency contacts

8. Appendix 3 - Reporting Templates: Standard forms for required progress reports and incident reporting