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1. Study Title and Research Team: Clear identification of the research study and contact information for all responsible parties
2. Introduction: Brief overview of the study and purpose of the consent form
3. Purpose of the Study: Detailed explanation of research objectives and importance
4. Study Procedures: Step-by-step description of what participation involves and expected duration
5. Risks and Discomforts: Clear explanation of potential risks, side effects, or inconveniences
6. Benefits: Description of direct and indirect benefits to participant and society
7. Data Protection and Confidentiality: Explanation of how personal data will be collected, stored, used, and protected
8. Costs and Compensation: Information about any costs or compensation for participation
9. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time
10. Contact Information: Details for questions, concerns, or emergencies
11. Declaration of Consent: Formal statement of consent with signature blocks for participant and researcher
1. Medical Care and Insurance: Required when research involves medical procedures or potential health risks
2. Future Use of Data/Samples: Needed when collected data or samples might be used in future research
3. Commercial Development: Required when research might lead to commercial products or patents
4. Genetic Testing Information: Necessary when study involves genetic analysis
5. Photography/Video Recording Consent: Required when study involves audio/visual recording
6. Third Party Data Sharing: Needed when data will be shared with other researchers or institutions
7. Special Population Considerations: Required for vulnerable populations (minors, impaired capacity)
8. Covid-19 Specific Measures: Needed during pandemic conditions for in-person research
1. Detailed Study Protocol: Technical description of research procedures and timeline
2. Participant Rights Summary: Simplified overview of participant rights under Swiss law
3. Data Processing Details: Technical details about data handling, storage, and protection measures
4. Emergency Procedures: Detailed emergency protocols and contact information
5. Withdrawal Procedures: Detailed process for withdrawing from the study
6. Glossary of Terms: Definitions of technical or medical terms used in the consent form
7. Research Team Credentials: Qualifications and roles of key research team members
Research Institution
Principal Investigator
Research Team
Participant
Legal Representative
Ethics Committee
Personal Data
Sensitive Personal Data
Data Processing
Anonymization
Pseudonymization
Informed Consent
Study Protocol
Clinical Trial
Adverse Event
Research Procedures
Biological Sample
Genetic Data
Data Controller
Data Processor
Withdrawal
Compensation
Confidentiality
Data Protection
Study Documentation
Research Results
Secondary Use
Data Access
Data Storage
Data Transfer
Research Purpose
Risk
Benefit
Emergency Contact
Regulatory Authorities
Voluntary Participation
Data Protection
Privacy
Confidentiality
Risk Disclosure
Benefits
Compensation
Withdrawal Rights
Medical Care
Emergency Procedures
Insurance Coverage
Data Collection
Data Storage
Data Processing
Data Sharing
Rights and Obligations
Consent Declaration
Contact Information
Duration and Timeline
Research Procedures
Sample Collection
Future Use
Publication Rights
Intellectual Property
Complaints Procedure
Termination
Amendments
Governing Law
Dispute Resolution
Healthcare
Pharmaceutical
Biotechnology
Academic Research
Clinical Research
Medical Devices
Psychology
Social Sciences
Market Research
Educational Research
Sports Science
Neuroscience
Behavioral Science
Legal
Research & Development
Clinical Operations
Regulatory Affairs
Ethics & Compliance
Data Protection
Quality Assurance
Medical Affairs
Clinical Research
Human Subject Protection
Research Administration
Research Director
Principal Investigator
Clinical Trial Manager
Research Ethics Officer
Data Protection Officer
Research Coordinator
Clinical Research Associate
Legal Counsel
Compliance Officer
Medical Director
Study Nurse
Research Administrator
Quality Assurance Manager
Regulatory Affairs Manager
Ethics Committee Member
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