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1. Equipment and Facilities: Details of research facilities and equipment usage when specific infrastructure is required

2. Personnel Requirements: Specific staffing requirements and qualifications when key personnel are critical

3. International Collaboration: Additional terms for cross-border research activities when multiple jurisdictions are involved

4. Regulatory Compliance: Industry-specific compliance requirements for regulated sectors

5. Data Protection: Enhanced data protection provisions when handling sensitive personal or medical data

6. Commercialization Rights: Terms for commercial exploitation when market deployment is anticipated

7. Background IP License: Detailed licensing terms when significant background IP is being used

8. Third-Party Rights: Provisions regarding third-party contractors or collaborators when external parties are involved

9. Insurance Requirements: Specific insurance provisions for high-risk research activities

10. Export Control: Export control compliance terms when dealing with controlled technologies or international transfers

1. Technical Specifications: Detailed technical requirements and research parameters

2. Project Plan: Comprehensive project timeline, milestones, and deliverables

3. Budget Breakdown: Detailed financial projections and cost allocations

4. Background IP Schedule: List of pre-existing intellectual property brought to the project

5. Key Personnel: List of essential team members and their roles

6. Research Protocols: Detailed research methodologies and procedures

7. Equipment Schedule: List of key equipment and facilities to be used

8. Reporting Templates: Standard formats for progress reports and documentation

9. Quality Assurance Procedures: Quality control and validation processes

10. Risk Management Plan: Identified risks and mitigation strategies