The Online Consent Form For Research is essential for any research activity involving human participants in Indonesia where consent is obtained electronically. This document type has become increasingly important with the rise of digital research methodologies and remote data collection. It must comply with Indonesia's Law No. 11 of 2008 on Electronic Information and Transactions, as well as relevant research ethics and data protection regulations. The form should be used whenever researchers need to obtain documented consent from participants in online or digital research settings. It includes crucial information about the research purpose, methodology, data handling procedures, participant rights, and privacy protections. The document is particularly relevant in the context of Indonesia's growing digital research landscape and the need for standardized, legally-compliant consent procedures.
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1. 1. Parties: Identification of the research institution/researcher and the research participant
2. 2. Background: Brief introduction to the research project and its purpose
3. 3. Definitions: Clear definitions of key terms used in the consent form
4. 4. Research Description: Detailed explanation of the research procedures, duration, and what participation involves
5. 5. Participant Rights: Clear statement of participant rights including the right to withdraw and access their data
6. 6. Risks and Benefits: Description of potential risks and benefits of participation in the research
7. 7. Data Collection and Privacy: Details about what data will be collected and how it will be protected
8. 8. Confidentiality Measures: Information about how participant confidentiality will be maintained
9. 9. Data Storage and Retention: Description of how and where data will be stored, and for how long
10. 10. Electronic Consent Declaration: Formal declaration of consent and acknowledgment of electronic signature validity
1. Compensation: Include when participants will receive payment or reimbursement for participation
2. Medical Disclaimer: Include for health-related research or when collecting health data
3. Future Research Use: Include when data might be used for future research projects
4. International Data Transfer: Include when data will be transferred outside Indonesia
5. Audio/Video Recording Consent: Include when research involves recording of participants
6. Commercial Use Declaration: Include when research has potential commercial applications
1. Appendix A: Research Project Summary: Detailed description of the research project, methodology, and timeline
2. Appendix B: Data Protection Measures: Technical and organizational measures for data protection
3. Appendix C: Participant Information Sheet: Detailed information about the research in lay terms
4. Appendix D: Contact Information: Complete contact details for researchers, ethics committee, and data protection officer
5. Appendix E: Withdrawal Form: Template form for participants to withdraw from the research
Relevant legal definitions
Clauses
Relevant Industries
Academic Research
Healthcare Research
Social Sciences
Market Research
Clinical Trials
Educational Research
Psychological Research
Technology Research
Pharmaceutical Research
Public Health
Environmental Research
Relevant Teams
Research & Development
Legal & Compliance
Data Protection
Ethics & Governance
Clinical Operations
Academic Affairs
Information Security
Research Administration
Quality Assurance
Participant Relations
Relevant Roles
Research Director
Principal Investigator
Research Ethics Officer
Data Protection Officer
Research Coordinator
Clinical Trial Manager
Research Compliance Manager
Legal Counsel
Research Administrator
Ethics Committee Chair
Research Methodology Expert
Data Security Officer
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