Consent Form For Research

Consent Form For Research Template for Singapore

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Key Requirements PROMPT example:

"I need a Consent Form For Research for a medical study at Singapore General Hospital involving collection of blood samples from elderly participants, with specific provisions for data sharing with our research partners in Australia and clear explanation of withdrawal rights."

Document background

The Consent Form For Research is a crucial document required by Singapore law before conducting any human subject research. It serves as a protective mechanism for both researchers and participants, ensuring transparent communication of research procedures and compliance with local regulations. The form must adhere to the PDPA, HBRA, and relevant ethical guidelines, while clearly documenting the participant's voluntary agreement to participate in the study. It typically includes detailed information about the research purpose, methodology, risks, benefits, confidentiality measures, and participant rights.

Suggested Sections

1. Title and Introduction: Research study title, institution details, and principal investigator information

2. Purpose of Research: Clear explanation of research objectives and methodology

3. Participant Requirements: What is expected from participants, including time commitment

4. Risks and Benefits: Detailed description of potential risks and benefits of participation

5. Confidentiality Statement: How personal information will be protected and used

6. Voluntary Participation: Statement about voluntary nature and right to withdraw

7. Contact Information: Details for researchers and ethics committee contacts

8. Declaration of Consent: Formal consent statement and signature blocks

Optional Sections

1. Compensation Information: Details about any payment or reimbursement for participation in the research

2. Medical Care Provisions: Information about available medical care for research-related injuries and associated costs

3. Future Use of Data: Information about data retention and potential use in future research studies

4. Audio/Video Recording Consent: Specific consent for recording participation in research activities

Suggested Schedules

1. Detailed Research Protocol: Technical details of the research methodology and procedures

2. Participant Information Sheet: Detailed information about the study written in lay terms

3. Medical Procedures List: Comprehensive list of medical procedures involved in the research

4. Data Protection Details: Specific information about data handling procedures and protection measures

Authors

Alex Denne

Head of Growth (Open Source Law) @ tiktok��˰� | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

alex.den.21@genieai.co

Relevant legal definitions

Clauses

Relevant Industries

Healthcare and Medical Research
Academic Institutions
Pharmaceutical Industry
Psychology and Behavioral Sciences
Social Sciences

Relevant Teams

Research & Development
Legal
Ethics Committee
Data Protection
Clinical Operations

Relevant Roles

Research Director
Principal Investigator
Research Ethics Officer
Clinical Trial Manager
Data Protection Officer

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Let's create your Consent Form For Research

Authors

Alex Denne

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