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Written Consent Form
"I need a Written Consent Form for my medical research study in Singapore, which will involve collecting blood samples from 100 participants starting March 2025, ensuring compliance with both PDPA and Human Biomedical Research Act requirements."
1. Identification of Parties: Details of the person giving consent and the organization/entity receiving consent
2. Purpose of Consent: Clear explanation of what the consent is being sought for
3. Scope of Consent: Specific details of what is being consented to
4. Declaration: Statement confirming voluntary consent and understanding
5. Signature Block: Space for signature, date, and witness details
1. Withdrawal Rights: Information about right to withdraw consent, use when PDPA applies
2. Risk Disclosure: Details of potential risks, use for medical/research consent
3. Third Party Disclosure: Information about sharing with third parties, use when data will be shared
4. Duration of Consent: Temporal limits of consent, use when consent has expiry
1. Details of Processing Activities: Detailed list of specific activities covered by consent
2. Privacy Policy: Organization's privacy policy when personal data is involved
3. Supporting Documents: Any relevant documentation referenced in main consent form
Authors
Purpose and Scope
Rights and Obligations
Data Collection
Data Use
Data Disclosure
Withdrawal Rights
Duration
Confidentiality
Privacy Protection
Third Party Sharing
Record Keeping
Access Rights
Security Measures
Communication
Representation and Warranties
Acknowledgment
Liability
Governing Law
Witness Requirements
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