Medical Non Disclosure Agreement Template for Switzerland

1. International Data Transfers: Required when confidential information may be transferred outside Switzerland, addressing cross-border data protection requirements

2. Research and Clinical Trial Provisions: Needed when the NDA relates to medical research or clinical trials, incorporating requirements from the Human Research Act

3. Electronic Health Records Handling: Required when dealing with electronic health records, incorporating EPRA requirements

4. Third Party Access: Needed when other healthcare providers, researchers, or service providers may need access to the confidential information

5. Insurance and Liability: Optional section addressing insurance requirements and liability limitations for data breaches

6. Publication Rights: Required for research-related agreements where publication of findings may be relevant

7. Cantonal Specific Requirements: Needed when activities fall under specific cantonal health regulations

1. Schedule 1: Categories of Confidential Information: Detailed listing of types of confidential medical information covered by the agreement

2. Schedule 2: Approved Security Measures: Specific technical and organizational measures required for data protection

3. Schedule 3: Authorized Personnel: List of individuals authorized to access confidential information and their access levels

4. Schedule 4: Data Processing Procedures: Detailed procedures for handling and processing confidential medical information

5. Appendix A: Breach Notification Procedures: Step-by-step procedures for handling and reporting confidentiality breaches

6. Appendix B: Compliance Checklist: Checklist ensuring compliance with Swiss medical privacy and data protection requirements