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Online Consent Form For Research

Online Consent Form For Research for Singapore

Online Consent Form For Research Template for Singapore

A legally compliant online consent form used in Singapore for obtaining informed consent from research participants. The document adheres to Singapore's Personal Data Protection Act (PDPA), Human Biomedical Research Act (HBRA), and relevant research ethics guidelines. It ensures proper documentation of participant consent while protecting their rights and personal data in digital format.

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Online Consent Form For Research

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What is a Online Consent Form For Research?

The Online Consent Form For Research is a crucial document in Singapore's research landscape, designed to meet the stringent requirements of local data protection and research ethics regulations. It enables researchers to obtain and document informed consent from participants in a digital format, while ensuring compliance with the PDPA, HBRA, and institutional review board requirements. This document is particularly relevant in the current digital age where remote research participation is increasingly common, requiring secure and legally valid electronic consent processes.

What sections should be included in a Online Consent Form For Research?

1. Study Information: Details of the research study, purpose, and procedures

2. Participant Rights: Rights of research participants, including withdrawal and data access

3. Data Protection: How personal data will be collected, used, stored, and protected in accordance with PDPA requirements

4. Risks and Benefits: Potential risks and benefits of participation in the research study

5. Contact Information: Details of researchers, institutional review board, and support contacts

6. Consent Declaration: Explicit consent statements and electronic signature section compliant with Electronic Transactions Act

What sections are optional to include in a Online Consent Form For Research?

1. Compensation Information: Details of any payment or reimbursement for participation, included when compensation is offered

2. Medical Procedures: Specific medical procedures involved, included for clinical research under HBRA

3. Future Research Use: Consent for future use of data/samples, included for longitudinal studies or biobank research

4. Third Party Access: Information about sharing with external parties or international transfers, included when applicable

What schedules should be included in a Online Consent Form For Research?

1. Detailed Study Protocol: Comprehensive description of research methodology and procedures

2. Participant Information Sheet: Simplified explanation of the study in lay terms with all required disclosures

3. Data Protection Notice: Detailed information about data handling practices in compliance with PDPA

4. Withdrawal Form: Template form for participants to withdraw from the study at any time

Authors

Alex Denne

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

Jurisdiction

Singapore

Publisher

tiktok成人版

Document Type

Consent Form

Sector

Research & Development

Cost

Free to use
Relevant legal definitions






























Clauses






























Industries

Personal Data Protection Act (PDPA): Singapore's primary data protection legislation governing the collection, use, and disclosure of personal data. Key considerations include requirements for valid consent, participants' data rights, and data protection obligations.

Human Biomedical Research Act (HBRA): Legislation specifically governing human biomedical research in Singapore, covering informed consent requirements, research subject protection, and Institutional Review Board oversight for human subjects and biological materials research.

Singapore Guidelines on Good Clinical Practice: Guidelines specifically for clinical trials and medical research, detailing standards for obtaining informed consent and documentation requirements in research settings.

Electronic Transactions Act: Legislation establishing the legal framework for electronic transactions in Singapore, including provisions for the validity of electronic records and signatures in consent processes.

National Healthcare Group DSRB Guidelines: Domain-specific guidelines establishing ethical requirements for research, including detailed consent procedures and participant protection measures in healthcare research.

International Research Guidelines: Key international standards like the Declaration of Helsinki that provide ethical principles for medical research involving human subjects and must be considered alongside local regulations.

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