The Experiment Consent Form is a crucial legal document required for any research involving human subjects in the Philippines. It serves as both a protective measure and an informational tool, ensuring that research participants are fully informed about their involvement in a study while safeguarding their rights under Philippine law. The document must comply with the Data Privacy Act of 2012, Philippine National Ethical Guidelines for Health Research, and other relevant local regulations. It is essential for any organization conducting research, clinical trials, or experiments involving human subjects, whether in academic, medical, or commercial settings. The form typically includes detailed information about the study's purpose, procedures, risks, benefits, confidentiality measures, and participant rights, while also providing clear documentation of informed consent as required by Philippine regulatory authorities.
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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 Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time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
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