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Research Data Sharing Agreement
"I need a Research Data Sharing Agreement between University of Cape Town and Stellenbosch University for sharing anonymized clinical trial data, with strict POPIA compliance requirements and provisions for joint publication rights."
1. Parties: Identification and details of the data provider and data recipient organizations
2. Background: Context of the research project and purpose of the data sharing arrangement
3. Definitions: Definitions of key terms including 'Research Data', 'Personal Information', 'Processing', 'Security Measures', and other relevant terms
4. Purpose and Scope: Detailed description of the purpose for which the data will be shared and used, including research objectives
5. Data Protection Compliance: Obligations under POPIA and other relevant data protection laws, including data minimization and purpose limitation principles
6. Data Transfer and Security: Protocols for secure data transfer, storage, and handling, including technical and organizational measures
7. Use Restrictions: Limitations on how the shared data may be used, including prohibitions on unauthorized use or sharing
8. Confidentiality: Obligations to maintain confidentiality of the shared data and research information
9. Intellectual Property Rights: Ownership and intellectual property rights related to the original data and derived research outputs
10. Duration and Termination: Term of the agreement and circumstances under which it can be terminated
11. Return or Destruction of Data: Requirements for handling shared data upon termination of the agreement
12. General Provisions: Standard legal clauses including governing law, dispute resolution, and entire agreement provisions
1. Commercial Use: Required when there is potential for commercial exploitation of research results
2. International Transfer Provisions: Required when data will be transferred outside South Africa
3. Publication Rights: Needed when parties wish to specify rights and procedures for publishing research results
4. Cost Sharing: Include when there are costs associated with data preparation or sharing that need to be allocated
5. Third Party Rights: Required when third parties may have rights in the data or derived research
6. Ethics Committee Approval: Necessary when research involves human subjects or requires ethical clearance
7. Data Quality and Validation: Include when specific data quality standards need to be maintained
8. Insurance and Indemnity: Required for high-risk research or where significant liability concerns exist
1. Schedule 1: Description of Research Data: Detailed description of the data sets to be shared, including format, fields, and metadata
2. Schedule 2: Security Requirements: Technical specifications for data security measures and protocols
3. Schedule 3: Authorized Personnel: List of authorized individuals who may access and process the shared data
4. Schedule 4: Data Processing Procedures: Step-by-step procedures for data handling, processing, and analysis
5. Schedule 5: Ethics Approvals: Copies of relevant ethics committee approvals and conditions
6. Appendix A: Data Transfer Protocol: Technical specifications for secure data transfer methods
7. Appendix B: Incident Response Plan: Procedures for handling data breaches or security incidents
Authors
Healthcare
Academic Research
Pharmaceutical
Biotechnology
Information Technology
Environmental Science
Social Sciences
Medical Research
Education
Public Health
Data Analytics
Agriculture
Clinical Research
Legal
Research & Development
Compliance
Information Security
Data Protection
Research Operations
Clinical Operations
Scientific Affairs
Information Technology
Research Ethics
Data Management
Research Administration
Regulatory Affairs
Research Director
Data Protection Officer
Chief Scientific Officer
Research Coordinator
Legal Counsel
Compliance Manager
Principal Investigator
Research Ethics Officer
Information Security Manager
Research Administrator
Chief Research Officer
Data Manager
Research Compliance Officer
Project Manager
Chief Technology Officer
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