Online Consent Form For Research

Online Consent Form For Research Template for Denmark

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Document background

The Online Consent Form For Research is a crucial document required for any research involving human participants in Denmark. It serves as a legal and ethical foundation for research activities, ensuring compliance with the Danish Act on Research Ethics Review, the Danish Data Protection Act, and EU GDPR requirements. This document is mandatory before commencing any research project involving human subjects and must be obtained in a manner that demonstrates clear, informed, and voluntary consent. The form must detail the research purpose, methodology, data handling practices, and participant rights, while being accessible through digital platforms. It's particularly important in the context of Denmark's strong emphasis on data protection and research ethics, requiring specific provisions for electronic consent collection and documentation.

Suggested Sections

1. Research Project Information: Title and identification of the research project, including responsible institution and principal investigator details

2. Researcher Contact Information: Complete contact details of the research team, including principal investigator and data protection officer

3. Purpose of the Research: Clear explanation of research objectives and potential benefits to society/science

4. Participation Details: Description of what participation involves, including time commitment, activities, and data collection methods

5. Data Collection and Processing: Detailed information about what personal data will be collected and how it will be processed, stored, and protected

6. Participant Rights: Explanation of all participant rights under GDPR and Danish law, including right to withdraw

7. Risks and Benefits: Clear description of any potential risks and benefits of participation

8. Voluntary Participation: Statement emphasizing voluntary nature of participation and right to withdraw

9. Data Protection Measures: Description of technical and organizational measures to protect participant data

10. Consent Declaration: Explicit consent statements with electronic signature mechanism

Optional Sections

1. Medical Information: Required if the research involves collection of health data or medical procedures

2. Commercial Interests: Required if the research has commercial sponsors or potential commercial applications

3. International Data Transfer: Required if data will be transferred outside the EU/EEA

4. Future Research Use: Optional section for consent to use data in future research projects

5. Compensation Information: Required if participants receive payment or compensation

6. Audio/Video Recording: Required if the research involves recording of participants

7. Biological Samples: Required if the research involves collection of biological samples

Suggested Schedules

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

2. Data Processing Activities: Detailed list of all data processing activities and purposes

3. Privacy Notice: Detailed privacy notice compliant with GDPR Article 13/14

4. Withdrawal Form: Template form for participants to withdraw from the study

5. Contact List: Complete list of relevant contacts including ethics committee and data protection authorities

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