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Consent And Indemnity Form
"I need a Consent and Indemnity Form for our upcoming medical research study in Singapore, starting March 2025, which will involve collecting sensitive health data from participants and conducting experimental treatments, requiring both informed consent and protection against potential claims."
1. Introduction and Parties: Identifies all parties involved and their details
2. Definitions: Key terms used throughout the document
3. Purpose of Consent: Clear statement of what is being consented to
4. Scope of Indemnity: Specific details of indemnification coverage
5. Duration: Period for which consent and indemnity remain valid
6. Execution: Signature blocks and witnessing requirements
1. Consideration: Details of any payment or value exchange - include when there is monetary or value consideration involved
2. Revocation Rights: Terms for withdrawing consent - include when consent needs to be revocable
3. Insurance Requirements: Specific insurance obligations - include when indemnity needs to be backed by insurance
1. Schedule of Specific Activities: Detailed list of activities covered by consent
2. Schedule of Indemnified Parties: List of additional parties covered by indemnity
3. Risk Disclosure: Detailed explanation of risks being assumed
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