Online Consent Form For Research

Online Consent Form For Research Template for Philippines

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Key Requirements PROMPT example:

"I need an Online Consent Form For Research for a clinical study on diabetes management in Manila, starting March 2025, which will involve collecting sensitive health data and sharing anonymized results with international research partners."

Document background

The Online Consent Form For Research is a crucial document required for any research involving human participants in the Philippines. It serves as a legal and ethical foundation for research activities, ensuring compliance with the Data Privacy Act of 2012 (RA 10173), Electronic Commerce Act of 2000 (RA 8792), and research ethics guidelines established by Philippine regulatory bodies. This document should be used whenever researchers need to obtain informed consent from participants through digital means, whether for academic, medical, or commercial research purposes. It includes comprehensive information about the research project, participant rights, data handling procedures, and privacy protections, while ensuring the validity of electronic consent in accordance with Philippine law. The form is particularly relevant in the current digital age, where remote research participation has become increasingly common.

Suggested Sections

1. Title and Research Information: Research title, principal investigator(s), and affiliated institution(s)

2. Purpose of the Study: Clear explanation of research objectives and importance

3. Participant Requirements: Description of what participation involves, including time commitment and activities

4. Risks and Benefits: Clear explanation of potential risks and benefits of participation

5. Data Privacy and Confidentiality: Information about data collection, storage, protection, and usage in compliance with the Data Privacy Act

6. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time

7. Contact Information: Details of researchers, ethics committee, and data privacy officer

8. Declaration of Consent: Explicit consent statements and electronic signature mechanism

Optional Sections

1. Compensation Information: Details about any compensation or reimbursement, used when participants will receive payment or compensation

2. Medical Procedures: Description of any medical procedures involved, required when research involves medical interventions

3. Future Use of Data: Information about potential future use of research data, included when data might be used for future studies

4. Third-Party Data Sharing: Details about sharing data with other researchers or institutions, included when data sharing is planned

5. Special Population Considerations: Additional protections and considerations for vulnerable populations, required when involving minors, elderly, or vulnerable groups

6. Commercial Implications: Information about potential commercial applications of research, included when research has possible commercial outcomes

Suggested Schedules

1. Detailed Research Protocol: Comprehensive description of research methodology and procedures

2. Data Processing Information: Detailed information about data handling procedures and privacy protection measures

3. Participant Rights: Comprehensive list of participant rights under Philippine law and research ethics guidelines

4. Withdrawal Procedures: Detailed procedures for withdrawing from the study and handling of collected data

5. Emergency Contact Protocol: Detailed procedures and contact information for emergencies or concerns

6. Glossary of Terms: Definitions of technical terms and concepts used in the consent form

Authors

Alex Denne

Head of Growth (Open Source Law) @ ��Ƶ | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

alex.den.21@genieai.co

Relevant legal definitions

Clauses

Relevant Industries

Healthcare

Education

Pharmaceuticals

Technology

Social Sciences

Psychology

Market Research

Clinical Research

Biotechnology

Public Health

Environmental Science

Agricultural Research

Relevant Teams

Research Operations

Legal

Compliance

Data Protection

Ethics Review

Clinical Operations

Research Administration

Quality Assurance

Risk Management

Information Technology

Relevant Roles

Research Director

Principal Investigator

Research Coordinator

Ethics Committee Member

Data Protection Officer

Research Compliance Officer

Legal Counsel

Research Administrator

Clinical Trial Manager

Research Ethics Officer

Research Project Manager

Human Subjects Protection Specialist

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