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1. Patient and Healthcare Provider Information: Identification of the patient, healthcare provider, and healthcare facility
2. Purpose of the Consent Form: Clear explanation of why consent is being sought and what it covers
3. Description of Procedure/Treatment: Detailed explanation of the proposed medical procedure, treatment, or care in plain language
4. Risks and Benefits: Comprehensive overview of potential risks, complications, and expected benefits
5. Alternative Options: Description of alternative treatments or procedures available to the patient
6. Data Processing Information: GDPR-compliant explanation of how patient data will be collected, used, and protected
7. Patient Rights: Statement of patient rights under Belgian law, including right to withdraw consent
8. Declaration of Consent: Explicit statement of consent with signature blocks for patient and healthcare provider
1. Research Participation: Required when the procedure is part of a clinical trial or research study
2. Interpreter Declaration: Required when consent discussions involve an interpreter for non-native speakers
3. Emergency Contact Information: Optional section for including emergency contact details
4. Photography/Recording Consent: Required when the procedure may involve medical photography or recording
5. Financial Information: Optional section for cost implications and insurance coverage
6. Specific Procedure Risks: Additional detailed risks section for complex procedures
1. Detailed Procedure Information: Technical medical information about the procedure/treatment
2. Post-Procedure Care Instructions: Detailed instructions for after-care and recovery
3. Privacy Notice: Detailed GDPR-compliant privacy notice explaining data processing practices
4. Patient Rights Document: Full explanation of patient rights under Belgian law
5. Medication Information: Details about required medications, if applicable
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