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Confidentiality Agreement In Research
"I need a Confidentiality Agreement In Research for a collaborative medical research project between our university and a pharmaceutical company, with specific provisions for handling patient data and potential patent rights, starting March 2025."
1. Parties: Identification of all parties involved in the research and bound by confidentiality
2. Background: Context of the research project and reason for confidentiality agreement
3. Definitions: Clear definitions of confidential information, research materials, and key terms
4. Scope of Confidentiality: Detailed description of what information is considered confidential
5. Obligations of Receiving Party: Specific duties regarding protection and non-disclosure
6. Permitted Disclosures: Circumstances under which confidential information may be disclosed
7. Term and Termination: Duration of confidentiality obligations and termination conditions
8. Return of Confidential Information: Requirements for returning or destroying confidential information
9. Governing Law: Specification of applicable laws and jurisdiction
1. Data Protection Measures: Specific security protocols for data handling when dealing with sensitive digital data or personal information
2. Publication Rights: Terms regarding academic publication of research results, typically used in academic research projects
3. Export Control Compliance: Provisions for compliance with export control regulations when research involves controlled technologies or international collaboration
4. HIPAA Compliance: Additional provisions for compliance with healthcare privacy regulations when research involves medical data
5. Intellectual Property Rights: Specific provisions regarding ownership and use of intellectual property arising from the research
1. Schedule A - Research Project Description: Detailed outline of the research project scope and objectives
2. Schedule B - Authorized Personnel List: List of individuals authorized to access confidential information
3. Schedule C - Security Protocols: Specific procedures for handling and storing confidential information
4. Schedule D - Data Management Plan: Procedures for data collection, storage, and destruction
5. Schedule E - Regulatory Compliance Requirements: List of applicable regulations and compliance requirements specific to the research
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