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Medical Non Disclosure Agreement
"I need a Medical Non-Disclosure Agreement for a clinical trial collaboration between our Austrian hospital and a pharmaceutical company, starting March 2025, with specific provisions for handling patient data and research findings."
1. Parties: Identification of the parties entering into the agreement, including their legal status and contact details
2. Background: Context of the agreement and the relationship between the parties
3. Definitions: Detailed definitions of key terms, particularly 'Confidential Information', 'Medical Data', 'Personal Data', and 'Processing'
4. Scope of Confidential Information: Detailed description of what constitutes confidential information, with specific reference to medical data categories
5. Obligations of Confidentiality: Core confidentiality obligations, including handling, storage, and protection of confidential information
6. Data Protection Compliance: Specific obligations under GDPR and Austrian data protection law, including handling of special category medical data
7. Permitted Disclosures: Circumstances under which confidential information may be disclosed, including legal requirements and authorized personnel
8. Security Measures: Required technical and organizational measures for protecting confidential information
9. Breach Notification: Procedures for reporting and handling any breaches of confidentiality
10. Return or Destruction of Information: Requirements for handling confidential information upon termination or request
11. Term and Termination: Duration of the agreement and termination provisions
12. Governing Law and Jurisdiction: Specification of Austrian law as governing law and jurisdiction for disputes
1. Audit Rights: Optional section granting rights to audit compliance with the agreement, recommended for high-sensitivity medical data
2. Insurance Requirements: Optional section requiring specific insurance coverage for data protection, recommended for high-risk situations
3. Third Party Access: Optional section governing access by third-party service providers or contractors, needed if third parties will be involved
4. International Data Transfers: Optional section addressing cross-border data transfers, required if data may be transferred outside the EU
5. Research Use Provisions: Optional section for situations where medical data may be used for research purposes
6. Publication Rights: Optional section addressing rights to publish findings, relevant for research or academic contexts
1. Schedule 1 - Categories of Confidential Information: Detailed listing of specific types of confidential information and medical data covered
2. Schedule 2 - Authorized Personnel: List of personnel authorized to access confidential information and their access levels
3. Schedule 3 - Security Protocols: Detailed technical and organizational security measures required
4. Schedule 4 - Data Processing Requirements: Specific requirements for processing medical data in compliance with GDPR
5. Appendix A - Breach Notification Procedures: Detailed procedures for reporting and handling confidentiality breaches
6. Appendix B - Data Retention Schedule: Specific timeframes for retention and destruction of different types of confidential information
Authors
Medizinische Daten (Medical Data)
Personenbezogene Daten (Personal Data)
Besondere Kategorien personenbezogener Daten (Special Categories of Personal Data)
Verarbeitung (Processing)
Verantwortlicher (Controller)
Auftragsverarbeiter (Processor)
Gesundheitsdaten (Health Data)
Betroffene Person (Data Subject)
Authorized Recipients
Security Breach
Permitted Purpose
Disclosing Party
Receiving Party
Representatives
Affiliate
Clinical Data
Research Data
Trade Secrets
Intellectual Property Rights
Medical Records
Patient Information
Clinical Trial Data
Technical Information
Proprietary Information
Business Information
Force Majeure
Effective Date
Term
Territory
Security Measures
Data Protection Laws
Applicable Healthcare Laws
Authorized Personnel
Professional Standards
Confidentiality Period
Data Protection
Medical Data Processing
Security Measures
Permitted Use
Disclosure Restrictions
Return of Information
Data Subject Rights
Breach Notification
Audit Rights
Term and Termination
Enforcement
Indemnification
Governing Law
Jurisdiction
Assignment
Severability
Survival
Third Party Rights
Force Majeure
Insurance
Regulatory Compliance
Healthcare Standards
Professional Obligations
Records Retention
Breach Remedies
Dispute Resolution
Notices
Entire Agreement
Amendments
Healthcare
Pharmaceuticals
Medical Devices
Biotechnology
Healthcare IT
Medical Research
Clinical Trials
Laboratory Services
Healthcare Consulting
Medical Education
Health Insurance
Digital Health
Medical Software
Healthcare Analytics
Medical Training
Legal
Compliance
Medical Affairs
Research & Development
Clinical Operations
Data Protection
Information Security
Healthcare Operations
Medical Information
Quality Assurance
Regulatory Affairs
Clinical Research
Information Technology
Ethics Committee
Data Management
Medical Director
Clinical Research Coordinator
Healthcare Privacy Officer
Data Protection Officer
Clinical Trial Manager
Medical Research Lead
Healthcare Compliance Manager
Medical Information Officer
Healthcare Technology Director
Medical Affairs Manager
Legal Counsel - Healthcare
Medical Data Manager
Chief Medical Officer
Healthcare Operations Director
Research Ethics Officer
Medical Software Developer
Healthcare Project Manager
Clinical Data Analyst
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