Experiment Consent Form

Experiment Consent Form Template for Singapore

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Key Requirements PROMPT example:

"I need an Experiment Consent Form for a psychology study at our university in Singapore, involving video recording of participants and collecting biometric data, which needs to be compliant with both PDPA and HBRA requirements."

Document background

The Experiment Consent Form is a crucial document required by Singapore law and research ethics guidelines before conducting any human subject research. It serves as both a legal protection and ethical safeguard, ensuring participants are fully informed about the research they're agreeing to join. The form must comply with Singapore's Human Biomedical Research Act, Personal Data Protection Act, and institutional review board requirements. It should be used whenever conducting research involving human subjects, whether in academic, medical, or commercial settings. The document includes detailed information about the study's purpose, procedures, risks, benefits, confidentiality measures, and participant rights.

Suggested Sections

1. Title and Institution Details: Name of study, institution, and principal investigators

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 Discomforts: Detailed description of potential risks and mitigation measures

5. Benefits: Potential benefits to participant and/or society

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

7. Voluntary Participation: Statement of voluntary nature and right to withdraw

8. Contact Information: Details for researchers and ethics board contacts

9. Signature Block: Space for participant and researcher signatures

Optional Sections

1. Compensation Details: Information about payment or reimbursement when participants receive compensation

2. Alternative Procedures: Other treatment options available for medical/clinical trials

3. Audio/Video Recording Consent: Specific consent for recording when recordings are part of the study

4. Future Use of Data: Consent for data use in future research when data might be used for future studies

Suggested Schedules

1. Detailed Procedure Description: Step-by-step explanation of experimental procedures

2. Medical History Form: Health information questionnaire if relevant to study

3. Emergency Contact Form: Contact information for emergencies

4. Photography/Recording Release: Specific permission for media usage

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

Academic Research
Healthcare
Pharmaceutical
Psychology
Technology

Relevant Teams

Research & Development
Legal
Ethics & Compliance
Clinical Operations
Data Protection

Relevant Roles

Research Director
Principal Investigator
Research Ethics Officer
Clinical Trial Manager
Research Coordinator
Legal Counsel

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Authors

Alex Denne

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