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Authorization To Release Protected Health Information Form
"I need an Authorization To Release Protected Health Information Form that allows my hospital to share patient data with a medical research institution in Brussels for a clinical trial running from March 2025 to December 2025, ensuring GDPR compliance and specific consent for genetic data processing."
1. Patient Information: Complete identification details of the patient including full name, date of birth, address, contact information, and national registry number
2. Healthcare Provider Information: Details of the healthcare provider/institution currently holding the medical records
3. Recipient Information: Information about the person or entity authorized to receive the medical information
4. Information to be Released: Specific description of what medical information is authorized for release, including date ranges and types of records
5. Purpose of Disclosure: Statement of the reason for releasing the medical information
6. Duration of Authorization: Specification of how long the authorization remains valid
7. Rights Statement: Information about the patient's rights under GDPR and Belgian law, including right to revoke authorization
8. Signatures and Date: Space for patient (or legal representative) signature, date, and witness signature if required
1. Legal Representative Authorization: Required only when someone other than the patient is authorizing the release, including details of their legal authority
2. Specific Consent for Sensitive Information: Additional authorization section for sensitive medical information (mental health, HIV status, genetic information) requiring explicit consent
3. Electronic Transmission Authorization: Specific authorization for electronic transmission of records, if applicable
4. Translation Declaration: Required when the form is provided in multiple languages, confirming the accuracy of translation
1. List of Specific Records: Detailed itemization of specific medical records to be released, allowing for precise selection
2. Fee Schedule: If applicable, breakdown of any administrative fees for record copying and transmission
3. Privacy Notice: Detailed GDPR privacy notice explaining how the information will be processed and protected
Authors
Data Subject
Data Controller
Data Processor
Healthcare Provider
Medical Records
Authorization Period
Legal Representative
Sensitive Personal Data
Health Data
Processing
Disclosure
Consent
Third Party
Electronic Health Record
Treatment
Medical Purpose
Data Protection Officer
Revocation
Confidential Communication
Patient Rights
Healthcare Institution
Personal Data
Special Categories of Data
Data Transfer
Privacy
Consent
Authorization
Information Access
Patient Rights
Data Processing
Confidentiality
Data Transfer
Duration
Revocation Rights
Record Specification
Identity Verification
Information Security
Liability
Compliance
Purpose Limitation
Data Subject Rights
Third Party Disclosure
Termination
Healthcare
Insurance
Medical Research
Pharmaceuticals
Elder Care
Mental Healthcare
Public Health
Healthcare Technology
Medical Education
Occupational Health
Legal
Compliance
Medical Records
Patient Administration
Data Protection
Healthcare Operations
Quality Assurance
Patient Services
Medical Administration
Information Management
Medical Director
Privacy Officer
Healthcare Administrator
Medical Records Manager
Compliance Officer
Legal Counsel
Data Protection Officer
Patient Relations Coordinator
Healthcare Provider
Insurance Claims Processor
Medical Research Coordinator
Clinical Trial Administrator
Medical Secretary
General Practitioner
Medical Specialist
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