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1. Title and Introduction: Clear identification of the document as a Survey Consent Form, including the study/survey title and organizing institution
2. Parties: Identification of the research institution/surveyor and the participant
3. Background: Brief overview of the survey purpose and context
4. Definitions: Clear definitions of key terms used in the consent form
5. Survey Purpose and Procedures: Detailed explanation of what the survey involves, its duration, and what will be required from participants
6. Data Collection and Protection: Description of what data will be collected and how it will be protected, stored, and used
7. Participant Rights: Clear statement of participant rights including right to withdraw, right to access data, and right to ask questions
8. Risks and Benefits: Description of any potential risks and benefits of participation
9. Voluntary Participation: Statement confirming that participation is voluntary and can be withdrawn at any time
10. Declaration of Consent: Formal consent statement and signature section
1. Compensation: Include when participants will receive payment or other compensation for participation
2. International Data Transfer: Include when data will be transferred outside Switzerland
3. Future Research Use: Include when data may be used for future research projects
4. Recording Procedures: Include when audio, video, or other recordings will be made
5. Medical Information: Include when the survey involves collection of medical or health-related data
6. Third Party Data Sharing: Include when data will be shared with third parties
1. Survey Questions Preview: Sample or full list of survey questions (if required by ethics committee)
2. Data Protection Policy: Detailed information about data protection measures and procedures
3. Contact Information Sheet: Detailed contact information for researchers, ethics committee, and data protection officer
4. Withdrawal Form: Template form for participants to withdraw from the study
Data Processing
Survey Administrator
Research Institution
Participant
Consent
Withdrawal
Confidentiality
Anonymous Data
Pseudonymized Data
Data Protection Officer
Ethics Committee
Research Project
Survey Response
Data Storage
Data Transfer
Sensitive Personal Data
Research Results
Participating Institution
Study Period
Data Subject Rights
Data Recipients
Research Team
Informed Consent
Voluntary Participation
Data Collection
Data Protection
Confidentiality
Participant Rights
Withdrawal Rights
Risk Disclosure
Benefits
Compensation
Data Storage and Retention
Data Sharing
International Transfer
Contact Information
Consent Declaration
Data Subject Rights
Liability
Governing Law
Research Procedures
Publication of Results
Future Research Use
Recording and Documentation
Ethics Approval
Termination
Amendment
Healthcare & Medical Research
Academic & Education
Market Research
Social Sciences
Psychology & Behavioral Studies
Public Policy & Government
Consumer Products & Services
Technology & Innovation
Financial Services
Pharmaceutical & Clinical Research
Legal
Research & Development
Compliance
Data Protection
Clinical Operations
Market Research
Academic Affairs
Research Ethics
Quality Assurance
Regulatory Affairs
Research Director
Data Protection Officer
Ethics Committee Member
Research Coordinator
Survey Administrator
Market Research Manager
Clinical Research Manager
Research Compliance Officer
Legal Counsel
Privacy Officer
Research Ethics Administrator
Project Manager
Research Methodology Expert
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