1. Special Conditions: Additional conditions specific to the research type or scope, used when the research involves sensitive subjects or special requirements

2. Ethical Compliance Requirements: Specific ethical guidelines and requirements, included when research involves human subjects or sensitive data

3. Reporting Requirements: Details of required progress reports or updates, included for longer-term or complex research projects

4. Safety Protocols: Specific safety requirements, included for research involving hazardous materials or procedures

5. Data Protection Requirements: Specific data handling and protection requirements, included when research involves personal or sensitive data

6. Institutional Collaboration Details: Information about partner institutions and their roles, included for multi-institutional research

7. Financial Considerations: Any financial terms or conditions, included when research involves funding or financial obligations

1. Research Protocol Summary: Brief overview of the approved research methodology and procedures

2. Team Members List: List of approved researchers and their roles in the project

3. Timeline Schedule: Detailed timeline of research activities and milestones

4. Required Documentation Checklist: List of documents that must be maintained during the research

5. Contact Information: List of key contacts at both the approving institution and research team

6. Institutional Review Board Approval: Copy of the IRB approval if applicable

7. Relevant Permits: Copies of any additional permits or approvals obtained