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Participant Consent Form
"I need a Participant Consent Form for a medical research study at Singapore General Hospital, involving collection of blood samples and genetic data from 100 participants, with specific provisions for data sharing with international research partners."
1. Title and Introduction: Study title, principal investigator, and institution details responsible for the research
2. Purpose of Research: Clear explanation of research objectives, methodology, and expected outcomes
3. Participation Requirements: Detailed explanation of what participation involves, including time commitment, procedures, and eligibility criteria
4. Risks and Benefits: Comprehensive overview of potential risks, discomforts, and benefits associated with participation
5. Confidentiality Statement: Details on how personal data will be collected, used, stored, and protected in accordance with PDPA 2012
6. Withdrawal Rights: Clear statement of participant's right to withdraw at any time and the process for withdrawal
7. Declaration of Consent: Formal consent statement and signature blocks for participant and researcher
1. Compensation Information: Details of any payment, reimbursement, or compensation provided for participation
2. Future Research Use: Information about potential future use of data or samples and associated consent options
3. Medical Care Provisions: Details of medical care provided during and after the study, including insurance coverage
4. Audio/Video Recording Consent: Specific consent for any audio or video recording during the research process
1. Schedule A - Detailed Study Procedures: Comprehensive step-by-step description of all research procedures and visits
2. Schedule B - Contact Information: List of all relevant contact persons, including researchers, ethics committee, and emergency contacts
3. Schedule C - Glossary of Terms: Definitions and explanations of technical or medical terms used in the consent form
4. Schedule D - Rights Under PDPA: Detailed explanation of participant rights under Singapore's Personal Data Protection Act
Authors
Principal Investigator
Research Participant
Personal Data
Confidential Information
Research Protocol
Informed Consent
Study Procedures
Research Institution
Ethics Committee
Institutional Review Board
Data Protection Officer
Adverse Event
Withdrawal Rights
Research Team
Study Materials
Biological Samples
Data Processing
Third Party
Legal Representative
Compensation
Research Results
Publication Rights
Secondary Use
Follow-up Period
Purpose of Research
Voluntary Participation
Study Procedures
Duration of Participation
Risks and Discomforts
Benefits
Alternatives
Confidentiality
Data Protection
Data Storage and Usage
Withdrawal Rights
Compensation
Costs
Emergency Contact
Medical Care
Insurance Coverage
Publication Rights
Future Research Use
Third Party Access
Intellectual Property
Liability
Governing Law
Declaration and Acknowledgment
Witness Requirements
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