Short Consent Form For Research

Short Consent Form For Research Template for Singapore

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Key Requirements PROMPT example:

"I need a Short Consent Form For Research for a psychology study at our university in Singapore, involving collection of behavioral data from 50 participants, ensuring PDPA compliance and including specific clauses about video recording of participants."

Document background

The Short Consent Form For Research is a essential document required for conducting human subject research in Singapore. It serves as a legal and ethical safeguard ensuring that research participants are properly informed and voluntarily agree to participate in studies. This document must comply with Singapore's regulatory framework, including the PDPA and HBRA, while following institutional review board guidelines. It contains crucial information about the study's purpose, procedures, risks, benefits, and participant rights, presented in a clear and concise format accessible to the general public.

Suggested Sections

1. Study Title and Basic Information: Clear identification of the research study, principal investigators, and institution

2. Purpose of Research: Brief explanation of research objectives, importance, and potential impact

3. Participation Requirements: Detailed explanation of what will be expected from participants, including time commitment and procedures

4. Risks and Benefits: Clear disclosure of potential risks, discomforts, and benefits of participation

5. Confidentiality Statement: Explanation of how participant information will be protected and data security measures

6. Voluntary Participation: Statement confirming voluntary nature of participation and right to withdraw at any time

7. Contact Information: Details for questions or concerns, including researcher and IRB contact information

Optional Sections

1. Compensation Details: Information about payment, reimbursement, or other compensation for participation

2. Future Use of Data: Details about data retention, storage, and potential use in future research

3. Biological Samples: Information about collection, storage, and future use of biological samples

4. Audio/Video Recording: Details about recording procedures and data storage when applicable

5. Third-Party Access: Information about potential sharing of data with other researchers or institutions

Suggested Schedules

1. Detailed Study Procedures: Comprehensive step-by-step description of research procedures and timeline

2. Schedule of Visits: Detailed timeline of research activities and required participant visits

3. Withdrawal Form: Template form for documenting participant withdrawal from the study

4. Emergency Contact Information: List of emergency contacts and procedures in case of adverse events

Authors

Alex Denne

Head of Growth (Open Source Law) @ ��Ƶ | 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
Academic Institutions
Pharmaceutical
Biotechnology
Psychology

Relevant Teams

Research & Development
Legal
Ethics & Compliance
Clinical Operations
Data Protection

Relevant Roles

Research Director
Principal Investigator
Research Coordinator
Ethics Committee Member
Compliance Officer

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Authors

Alex Denne

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