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Consent And Waiver
"I need a Consent and Waiver document for my medical research facility in Singapore, covering patient consent for clinical trials and waiver of liability for non-adverse effects, to be implemented from March 2025."
1. Parties: Identification of all parties providing and receiving consent/waiver
2. Background: Context and circumstances leading to the consent/waiver
3. Definitions: Key terms used in the document
4. Scope of Consent: Explicit description of what is being consented to
5. Scope of Waiver: Clear description of rights being waived
6. Duration: Period for which consent/waiver remains valid
7. Governing Law: Specification of Singapore law as governing law
1. Data Protection Provisions: Required when personal data collection, use, or disclosure is involved
2. Consideration: Details of any payment or value exchange when waiver is given for consideration
3. Indemnification: Protection against future claims when additional legal protection is needed
1. Schedule of Rights Waived: Detailed list of specific rights being waived
2. Schedule of Consented Activities: Detailed list of activities being consented to
3. Schedule of Personal Data: List of personal data categories involved (if applicable)
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