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1. Publication Rights: Used when parties need to establish rules for publishing trial results or academic papers

2. Third Party Disclosure: Include when third party contractors or consultants will need access to confidential information

3. International Data Transfer: Required when confidential information will be transferred across borders

4. Intellectual Property Rights: Include when the trial may generate patentable innovations or intellectual property

5. Insurance and Indemnification: Used when specific risk allocation for information breaches needs to be addressed

6. Audit Rights: Include when one party requires rights to audit the other's compliance with confidentiality obligations

7. Competing Products/Research: Used when restrictions on involvement in competing research need to be addressed

1. Schedule 1 - Description of Clinical Trial: Detailed description of the clinical trial, including protocol number and trial phase

2. Schedule 2 - Authorized Personnel: List of authorized personnel who will have access to confidential information

3. Schedule 3 - Security Protocols: Detailed security measures and protocols for handling confidential information

4. Schedule 4 - Data Protection Requirements: Specific data protection requirements and compliance procedures

5. Appendix A - Form of Confidentiality Undertaking: Template confidentiality undertaking for individual researchers/staff

6. Appendix B - Information Classification Guidelines: Guidelines for classifying different types of confidential information

7. Appendix C - Breach Notification Procedures: Procedures to be followed in case of confidentiality breach