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1. Research Data Provisions: Additional provisions specifically for medical research data, used when the NDA covers research activities

2. International Transfer Provisions: Specific provisions for cross-border data transfers, required when medical data may be transferred outside the Netherlands

3. Audit Rights: Provisions allowing the disclosing party to audit the receiving party's compliance, recommended for high-sensitivity medical data

4. Insurance Requirements: Obligations to maintain specific insurance coverage, relevant for high-risk medical information

5. Sub-processor Provisions: Requirements for engaging sub-processors, needed when the receiving party may need to share data with third parties

6. Patient Consent Procedures: Specific procedures for handling patient consent, relevant when direct patient care is involved

7. Intellectual Property Rights: Provisions regarding IP rights in derived data or research findings, relevant for research contexts

1. Schedule 1 - Security Requirements: Detailed technical and organizational security measures required for protecting the medical information

2. Schedule 2 - Approved Sub-processors: List of pre-approved sub-processors and their specific roles (if applicable)

3. Schedule 3 - Data Processing Activities: Detailed description of permitted data processing activities and purposes

4. Schedule 4 - Contact Points: List of key contacts for security incidents, audits, and general communication

5. Appendix A - Data Categories: Detailed categorization of types of medical data covered by the agreement

6. Appendix B - Standard Operating Procedures: Procedures for handling specific types of medical information and security incidents