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1. Ethics and Compliance: Required when research involves human subjects, animal testing, or regulated industries

2. Data Protection: Detailed section needed when research involves personal or sensitive data processing

3. Publication Rights: Important for academic institutions or when public disclosure of research results is contemplated

4. Export Control: Required when research involves internationally controlled technology or materials

5. Background IP License: Needed when parties need to use each other's existing intellectual property

6. Third Party Rights: Required when research involves third party materials or collaboration

7. Insurance and Indemnity: Detailed section needed for high-risk research activities

8. Force Majeure: Extended clause needed for long-term research projects with significant external dependencies

1. Schedule 1: Research Proposal: Detailed technical description of the research project, methodology, and objectives

2. Schedule 2: Budget and Payment Schedule: Detailed breakdown of costs and payment milestones

3. Schedule 3: Timeline and Deliverables: Specific project milestones, deadlines, and deliverable specifications

4. Schedule 4: Key Personnel: List of key researchers and their qualifications

5. Schedule 5: Research Protocols: Detailed research methodologies and procedures

6. Schedule 6: Equipment and Materials: List of equipment and materials to be used or provided

7. Schedule 7: Reporting Templates: Standard formats for progress reports and final documentation

8. Appendix A: Background IP: List of relevant pre-existing intellectual property

9. Appendix B: Compliance Requirements: Specific regulatory or ethical requirements applicable to the research