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Confidentiality Agreement For Research Participants
"I need a Confidentiality Agreement For Research Participants for a medical research study at Oxford University starting in March 2025, which will involve collecting sensitive health data from approximately 200 participants over a 6-month period."
1. Parties: Identification of the research organization and participant
2. Background: Context of the research project and purpose of the agreement
3. Definitions: Key terms used throughout the agreement including Confidential Information, Research Project, and Permitted Purpose
4. Confidentiality Obligations: Core obligations regarding confidential information, including non-disclosure and security measures
5. Duration of Obligations: Time period for which confidentiality obligations remain in effect
6. Permitted Uses: Specific allowed uses of confidential information within the research context
7. Return of Information: Requirements for returning or destroying confidential information upon completion or termination
1. Medical Data Provisions: Additional provisions specific to handling medical data and compliance with healthcare regulations
2. Intellectual Property Rights: Provisions regarding ownership and use of intellectual property arising from the research
3. Publication Rights: Terms governing the publication of research findings and review procedures
1. Schedule 1 - Research Project Description: Detailed description of the research project, including objectives and methodology
2. Schedule 2 - Confidential Information Types: Comprehensive list of types of confidential information covered by the agreement
3. Schedule 3 - Data Processing Details: Specific details about personal data processing procedures and safeguards
4. Schedule 4 - Consent Form: Standard form for participant consent and acknowledgment of confidentiality obligations
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