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1. Subject Injury: Specific provisions for handling and compensation for research-related injuries, required when the trial involves higher risk procedures

2. Multi-Center Trial Provisions: Additional terms for coordination among multiple research sites, used in multi-center studies

3. Equipment and Supplies: Terms for provision and handling of specialized equipment or supplies, needed when sponsor provides specific equipment

4. Biological Materials: Provisions for handling biological samples and associated rights, required for trials involving specimen collection

5. Third Party Agreements: Terms governing relationships with external vendors or service providers, needed when external services are utilized

6. Post-Trial Access: Provisions for continued access to study treatment after trial completion, relevant for certain drug trials

7. Force Majeure: Provisions for handling unforeseen circumstances, particularly relevant post-COVID

8. Electronic Systems: Terms for use of electronic data capture or other technical systems, needed when specific systems are required

1. Schedule A - Protocol: Detailed clinical trial protocol including all amendments

2. Schedule B - Budget: Detailed financial terms, payment schedule, and cost breakdown

3. Schedule C - Payment Schedule: Timeline and conditions for payments

4. Schedule D - Required Reports: List and templates of required study reports and timelines

5. Schedule E - Form of Informed Consent: Approved informed consent form and process

6. Schedule F - Data Transfer Agreement: Specific terms for data sharing and transfer

7. Appendix 1 - Study Team: List of approved investigators and key study personnel

8. Appendix 2 - Timeline: Detailed study timeline and milestones

9. Appendix 3 - Quality Requirements: Specific quality control and assurance requirements

10. Appendix 4 - Safety Reporting: Procedures for adverse event reporting and safety monitoring