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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."
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
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
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
Participant
Principal Investigator
Research Institution
Personal Data
Sensitive Personal Data
Informed Consent
Research Protocol
Data Collection
Data Processing
Withdrawal
Institutional Review Board
Confidential Information
Research Materials
Study Procedures
Electronic Signature
Data Protection Officer
Research Team
Anonymization
Data Storage
Third Party
Research Results
Study Period
Compensation
Adverse Event
Privacy Notice
Consent Withdrawal
Data Subject Rights
Study Documentation
Research Ethics Committee
Voluntary Participation
Confidentiality
Data Collection and Use
Data Protection
Privacy
Rights and Responsibilities
Withdrawal Rights
Risk Disclosure
Benefits
Compensation
Emergency Procedures
Recording and Documentation
Data Storage and Security
Data Sharing
Future Research Use
Contact Information
Consent Declaration
Electronic Signature
Third Party Disclosure
Publication Rights
Termination
Governing Law
Dispute Resolution
Amendment Procedures
Language Declaration
Acknowledgment
Regulatory Compliance
Data Subject Rights
Retention Period
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