1. Special Categories Authorization: Additional authorization for sensitive information such as HIV status, mental health records, or genetic information

2. Research Purposes: Additional provisions when medical information will be used for research purposes

3. International Transfer: Specific provisions for when medical information will be transferred outside the EU

4. Electronic Communication Consent: Additional consent for sharing information via electronic means

5. Representative Authorization: Section for cases where a legal representative is acting on behalf of the patient

6. Emergency Contact: Optional inclusion of emergency contact information

7. Language Assistance: Documentation of any translation or interpretation services provided

1. Schedule A - Detailed Medical Records List: Itemized list of specific medical records to be released

2. Schedule B - Authorized Recipients: Complete list of all authorized recipients if multiple parties are involved

3. Schedule C - Data Processing Information: Detailed information about how the data will be processed, stored, and protected

4. Appendix 1 - Patient Rights Summary: Detailed explanation of patient rights under GDPR and German law

5. Appendix 2 - Privacy Notice: Detailed privacy notice as required by GDPR

6. Appendix 3 - Glossary: Definitions of medical and legal terms used in the document