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1. Parties: Identification of all parties to the agreement, including full legal names, addresses, and registration details where applicable
2. Background: Context of the agreement, nature of the medical information involved, and the relationship between the parties
3. Definitions: Detailed definitions of key terms, including 'Confidential Information', 'Medical Data', 'Personal Data', 'Processing', and other GDPR-specific terminology
4. Scope of Confidential Information: Detailed description of what constitutes confidential medical information under the agreement, including patient data, research data, and medical procedures
5. Obligations of Confidentiality: Core confidentiality obligations, including handling, storage, and protection of medical information
6. Data Protection Compliance: Specific obligations under GDPR and Belgian data protection law, including data processing principles and security measures
7. Permitted Disclosures: Circumstances under which confidential information may be disclosed, including legal requirements and patient consent
8. Term and Termination: Duration of the agreement and circumstances for termination
9. Return or Destruction of Confidential Information: Obligations regarding the handling of confidential information upon termination
10. Breach and Remedies: Consequences of breach and available remedies, including notification requirements for data breaches
11. Governing Law and Jurisdiction: Specification of Belgian law as governing law and jurisdiction for disputes
1. Third Party Access: Include when other parties (such as contractors or service providers) may need access to the confidential information
2. International Data Transfers: Include when medical data might be transferred outside the EU/EEA
3. Research and Publication Rights: Include when the agreement relates to medical research with potential publication implications
4. Insurance Requirements: Include when specific insurance coverage is required for handling sensitive medical data
5. Data Subject Rights: Include when the agreement involves processing of identifiable patient data, detailing how data subject requests will be handled
6. Audit Rights: Include when one party requires the right to audit the other's compliance with data protection and confidentiality obligations
1. Security Measures: Technical and organizational measures required for protecting medical data
2. Data Processing Details: Specific details about the types of medical data being processed, purposes, and processing activities
3. Authorized Personnel: List of authorized individuals or roles permitted to access the confidential medical information
4. Data Breach Response Plan: Procedures and contact details for handling data breach incidents
Healthcare
Pharmaceuticals
Biotechnology
Medical Devices
Healthcare Technology
Clinical Research
Medical Education
Healthcare Insurance
Medical Laboratory Services
Digital Health
Telemedicine
Healthcare Consulting
Legal
Compliance
Medical Affairs
Clinical Research
Data Protection
Information Security
Risk Management
Medical Records
Research & Development
Healthcare Operations
Quality Assurance
Regulatory Affairs
Medical Director
Chief Medical Officer
Clinical Research Coordinator
Data Protection Officer
Healthcare Privacy Officer
Medical Research Director
Clinical Trial Manager
Hospital Administrator
Medical Records Manager
Healthcare Compliance Officer
Medical Information Officer
Healthcare Legal Counsel
Medical Ethics Officer
Healthcare Risk Manager
Medical Practice Manager
Clinical Data Manager
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