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1. Commercialization Rights: Include when there's potential for commercial exploitation of research results

2. Equipment and Materials: Include when specific research equipment or materials are being provided

3. Ethics and Compliance: Include for research involving human subjects or requiring ethical approvals

4. Research Funding: Include when the license is tied to specific research funding arrangements

5. Quality Control: Include when specific quality standards or protocols must be followed

6. Transfer of Materials: Include when physical materials are being transferred for research

7. Reporting Requirements: Include when periodic research progress reports are required

8. Sub-licensing Rights: Include when licensee may need to involve third-party researchers

1. Schedule 1 - Licensed Material: Detailed description of the licensed intellectual property, materials, or methods

2. Schedule 2 - Research Plan: Detailed description of the approved research activities and methodologies

3. Schedule 3 - Fee Schedule: Any applicable license fees, maintenance fees, or other financial terms

4. Schedule 4 - Approved Researchers: List of authorized researchers if license is restricted to specific individuals

5. Appendix A - Data Processing Agreement: GDPR-compliant data processing terms if personal data is involved

6. Appendix B - Material Transfer Protocols: Specific procedures for handling and transferring research materials

7. Appendix C - Publication Protocol: Detailed procedures for publication review and approval