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1. Regulatory Compliance: Required when R&D involves regulated industries or products

2. Background IP License: Needed when existing IP is being licensed for use in the R&D

3. Clinical Trial Provisions: Required for R&D involving human subjects or clinical trials

4. Government Funding: Required when project receives government grants or funding

5. Export Control: Needed for international R&D collaboration or technology transfer

6. Commercialization Rights: Optional provisions for future commercialization of R&D results

7. Publication Rights: Required for academic collaborations or public research institutions

8. Equipment and Facilities: Needed when specific research facilities or equipment are provided

9. Student Involvement: Required when university students are involved in the R&D

1. Project Plan: Detailed timeline, milestones, and deliverables

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

3. Background IP: List and description of existing IP being brought to the project

4. Key Personnel: List of key researchers and their roles

5. Technical Specifications: Detailed technical requirements and specifications

6. Research Protocols: Detailed research methodologies and procedures

7. Form of Reports: Templates for progress and final reports

8. Equipment and Facilities: List and specifications of equipment and facilities to be used

9. Security Requirements: IT and physical security requirements for the project