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1. Research Institution and Participant Information: Identifies the research institution, principal investigators, and space for participant details
2. Research Project Overview: Brief description of the research project, its purpose, and expected duration
3. Participation Details: Explains what participation involves, including time commitment, activities, and any potential risks or benefits
4. Data Collection and Processing: Details of what data will be collected, how it will be used, stored, and processed in compliance with GDPR
5. Participant Rights: Explanation of rights under GDPR and research regulations, including right to withdraw, data access, and deletion
6. Voluntary Nature and Withdrawal: Statement confirming voluntary participation and right to withdraw without consequences
7. Contact Information: Details for reaching researchers, data protection officer, and ethics committee
8. Declaration of Consent: Clear statements of consent with checkboxes/electronic confirmation mechanisms
1. Medical Information: Required if research involves health data or medical procedures, including specific health-related consents
2. Audio/Video Recording Consent: Required if research involves recording participants
3. Genetic Data Processing: Required if research involves genetic testing or analysis
4. Third Party Data Sharing: Required if data will be shared with other research institutions or processors
5. Commercial Use of Research: Required if research results might be commercially exploited
6. International Data Transfers: Required if data will be transferred outside the EU/EEA
1. Detailed Research Protocol: Comprehensive description of research methodology and procedures
2. Data Protection Impact Assessment Summary: Summary of DPIA if required under GDPR for high-risk processing
3. List of Data Processors: If applicable, list of third parties processing research data
4. Privacy Notice: Detailed privacy information as required under GDPR Article 13/14
5. Withdrawal Form: Template form for participants to withdraw from the research
Academic Research
Healthcare
Pharmaceutical
Psychology
Social Sciences
Market Research
Clinical Trials
Biotechnology
Education
Technology Research
Consumer Behavior Research
Medical Devices
Legal
Research & Development
Clinical Operations
Regulatory Affairs
Data Protection
Ethics & Compliance
Research Administration
Information Technology
Privacy
Academic Affairs
Research Director
Principal Investigator
Research Ethics Officer
Data Protection Officer
Research Project Manager
Clinical Trial Coordinator
Research Compliance Manager
Legal Counsel
Research Administrator
Ethics Committee Member
Research Scientist
Research Assistant
Privacy Officer
Regulatory Affairs Manager
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骋别苍颈别鈥檚 Security Promise
Genie is the safest place to draft. Here鈥檚 how we prioritise your privacy and security.
Your documents are private:
We do not train on your data; 骋别苍颈别鈥檚 AI improves independently
All data stored on Genie is private to your organisation
Your documents are protected:
Your documents are protected by ultra-secure 256-bit encryption
We are ISO27001 certified, so your data is secure
Organizational security:
You retain IP ownership of your documents and their information
You have full control over your data and who gets to see it