The Confidential Disclosure Agreement In Clinical Research is essential when parties need to share sensitive information during clinical trials or research studies in Singapore. It is particularly relevant when handling patient data, research methodologies, or proprietary information in compliance with Singapore's regulatory framework. This agreement ensures that confidential information is protected while facilitating necessary collaboration between research institutions, pharmaceutical companies, and healthcare providers. It addresses specific requirements under Singapore law, including PDPA compliance and clinical research regulations.
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Key Requirements PROMPT example:
Confidential Disclosure Agreement In Clinical Research
"I need a Confidential Disclosure Agreement In Clinical Research between our research institution and a pharmaceutical company for a Phase II clinical trial starting in March 2025, with specific provisions for handling patient data across multiple hospital sites in Singapore."
1. Parties: Identification of all parties involved in the agreement, including full legal names and addresses
2. Background: Context of the clinical research and purpose of the confidentiality agreement
3. Definitions: Detailed definitions of key terms, especially 'Confidential Information', 'Clinical Trial', and 'Study Data'
4. Scope of Confidential Information: Detailed description of what constitutes confidential information under the agreement
5. Obligations of Confidentiality: Core confidentiality obligations and permitted uses of confidential information
6. Term and Termination: Duration of the agreement and conditions for termination
7. Return or Destruction of Confidential Information: Procedures for handling confidential information after agreement termination
1. Third Party Disclosure: Terms for sharing information with authorized third parties when third-party contractors or consultants are involved in the research
2. Cross-Border Data Transfer: Provisions for international data transfer when research involves multiple jurisdictions
3. Publication Rights: Terms regarding publication of research results when academic institutions are involved
4. Specific Data Protection Measures: Technical and organizational measures for data protection when handling sensitive personal or medical data
1. Schedule 1: Description of Clinical Trial: Detailed description of the clinical trial or research project
2. Schedule 2: Authorized Representatives: List of authorized personnel who may access confidential information
3. Schedule 3: Data Protection Protocols: Specific procedures for handling and protecting confidential information
4. Schedule 4: Required Notifications: List of circumstances requiring mandatory notification between parties
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