Online Consent Form For Research Template for Singapore

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Key Requirements PROMPT example:

Online Consent Form For Research

"I need an Online Consent Form For Research for a large-scale medical study across multiple Singapore hospitals, with specific clauses for collecting sensitive health data and biological samples, and the ability for participants to electronically sign through our hospital portal."

Document background
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.
Suggested Sections

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

Optional Sections

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

Suggested Schedules

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) @ Genie AI | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

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.

Teams

Employer, Employee, Start Date, Job Title, Department, Location, Probationary Period, Notice Period, Salary, Overtime, Vacation Pay, Statutory Holidays, Benefits, Bonus, Expenses, Working Hours, Rest Breaks,  Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination,  Severance Pay, Governing Law, Entire Agreemen

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