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1. Title and Document Identification: Clear identification of the document as an experiment consent form, including the study title and protocol number
2. Parties: Identification of the research institution/experimenter and the participant
3. Background Information: Brief overview of the research study and its purpose
4. Definitions: Clear definitions of technical terms and important concepts used in the document
5. Study Procedures: Detailed description of what participation involves, including time commitment and specific procedures
6. Risks and Discomforts: Clear explanation of potential risks, side effects, or discomforts
7. Benefits: Description of potential benefits to the participant and/or society
8. Costs and Compensation: Information about any costs involved and compensation provided
9. Confidentiality: Explanation of how personal information and data will be protected and used
10. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time
11. Contact Information: Details of who to contact for questions about the research or participants' rights
12. Declaration of Consent: Formal statement of consent and signature blocks
1. Alternative Treatments: Required when the experiment involves medical treatments where alternatives exist
2. Future Use of Information: Include when data might be used for future research or shared with other researchers
3. Commercial Applications: Required when research might lead to commercial products or patents
4. Biological Samples: Include when the study involves collecting and storing biological samples
5. Photography/Recording Consent: Required when the study involves taking photographs or making audio/video recordings
6. Translation Declaration: Include when the form is translated from English to local dialects
7. Guardian Consent: Required for participants who cannot legally consent for themselves
1. Schedule A - Detailed Study Protocol: Detailed description of the experimental procedures and timeline
2. Schedule B - Risk Disclosure: Comprehensive list of potential risks and mitigation measures
3. Schedule C - Rights of Research Participants: Detailed explanation of participant rights under Philippine law
4. Appendix 1 - Emergency Contact Information: Complete list of emergency contacts and procedures
5. Appendix 2 - Data Privacy Notice: Detailed information about data handling and privacy protection measures
6. Appendix 3 - Withdrawal Form: Form for participants to withdraw from the study if they choose
Healthcare
Pharmaceutical
Academic Research
Clinical Research
Psychology
Social Sciences
Medical Devices
Biotechnology
Public Health
Educational Research
Consumer Products Testing
Market Research
Legal
Research & Development
Clinical Operations
Regulatory Affairs
Ethics & Compliance
Data Protection
Medical Affairs
Project Management
Quality Assurance
Research Administration
Human Subject Protection
Research Director
Principal Investigator
Clinical Trial Manager
Research Ethics Officer
Data Protection Officer
Research Coordinator
Clinical Research Associate
Study Administrator
Legal Counsel
Regulatory Affairs Specialist
Human Subjects Protection Specialist
Research Compliance Officer
Medical Director
Research Project Manager
Ethics Committee Member
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