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General Consent Form
"I need a General Consent Form for my Singapore-based medical research company to obtain permission from participants for a clinical trial starting in March 2025, including data collection and storage provisions that comply with PDPA requirements."
1. Personal Information: Details of the person giving consent including name, identification number, contact information
2. Purpose of Consent: Clear explanation of what the consent is being given for and the legal basis under PDPA 2012
3. Scope of Consent: Specific details of what is being consented to, including collection, use, and disclosure of personal data
4. Duration of Consent: Period for which the consent remains valid and conditions for expiry
5. Rights and Obligations: Statement of rights including withdrawal of consent, access to personal data, and correction rights under PDPA
6. Declaration: Confirmation that the person understands and agrees to the terms of consent
1. Medical Information: Required when consent involves medical procedures or health information, subject to additional healthcare privacy requirements
2. Third Party Authorization: Details of authorized representatives or deputies, particularly relevant under Mental Capacity Act
3. Special Conditions: Any specific conditions, limitations, or exclusions to the consent
1. Schedule A - Personal Data Categories: Detailed list of personal data categories being collected, used, or disclosed
2. Schedule B - Authorized Uses: Comprehensive list of authorized uses and purposes for the personal data
3. Schedule C - Third Party Recipients: List of third parties who may receive or process the personal data
4. Schedule D - Data Protection Measures: Overview of security measures and safeguards for protecting personal data
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