The Consent Form For Research Questionnaire is an essential document required for any research involving human participants in Switzerland. It must comply with Swiss federal regulations, particularly the Federal Act on Data Protection (FADP/DSG) and the Human Research Act (HRA). This document should be used whenever conducting research that involves collecting data from human subjects through questionnaires or surveys. It includes comprehensive information about the research project, data protection measures, participant rights, and consent declarations. The form serves multiple purposes: ensuring legal compliance, protecting participant rights, documenting informed consent, and maintaining ethical research standards. It is particularly important in academic, medical, and social research contexts where personal data is collected and processed. The document must be reviewed by ethics committees and data protection officers before implementation.
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1. Title and Project Identification: Clear identification of the research project, institution, and form type
2. Parties: Identification of the research institution/researchers and the participant
3. Background: Brief overview of the research project and its purpose
4. Definitions: Clear explanations of technical terms and important concepts used in the form
5. Purpose of the Study: Detailed explanation of research objectives and expected outcomes
6. Study Procedures: Description of what participation involves, including time commitment and types of questions
7. Data Protection and Confidentiality: Explanation of how personal data will be collected, stored, used, and protected
8. Participant Rights: Clear statement of participant rights including withdrawal and data access rights
9. Risks and Benefits: Description of any potential risks and benefits of participation
10. Voluntary Nature of Participation: Statement confirming participation is voluntary and can be withdrawn
11. Contact Information: Details of researchers, supervisors, and ethics committee contacts
12. Declaration of Consent: Formal consent statement and signature section
1. Compensation: Details of any payment or compensation for participation, if applicable
2. Future Use of Data: Information about potential future use of data in other research projects
3. Commercial Applications: Information about potential commercial applications of research findings
4. Medical Information: Required for health-related research, including medical disclaimers and health-specific risks
5. Translation Statement: Required when the form is provided in multiple languages
6. Vulnerable Participants: Additional protections and information for vulnerable groups (minors, elderly, etc.)
7. Audio/Video Recording: Specific consent for recording if the research involves audio or video recording
1. Research Questionnaire: Copy of the actual questionnaire or survey to be completed
2. Participant Information Sheet: Detailed information about the research project and participation requirements
3. Data Protection Policy: Detailed explanation of data protection measures and procedures
4. Research Timeline: Schedule of research activities and important dates
5. Rights Summary: Summary of participant rights in simple, accessible language
6. Withdrawal Form: Template form for participants to withdraw from the study
Relevant legal definitions
Research Project
Questionnaire
Personal Data
Sensitive Personal Data
Data Processing
Anonymization
Pseudonymization
Research Institution
Principal Investigator
Ethics Committee
Participant
Informed Consent
Study Protocol
Data Controller
Data Processor
Research Team
Confidentiality
Data Protection
Withdrawal Rights
Data Storage
Data Retention Period
Research Results
Secondary Use
Data Subject Rights
Data Transfer
Questionnaire
Personal Data
Sensitive Personal Data
Data Processing
Anonymization
Pseudonymization
Research Institution
Principal Investigator
Ethics Committee
Participant
Informed Consent
Study Protocol
Data Controller
Data Processor
Research Team
Confidentiality
Data Protection
Withdrawal Rights
Data Storage
Data Retention Period
Research Results
Secondary Use
Data Subject Rights
Data Transfer
Clauses
Consent Declaration
Voluntary Participation
Data Protection
Confidentiality
Purpose of Research
Research Procedures
Rights and Obligations
Risk Disclosure
Benefits
Withdrawal Rights
Data Storage and Security
Data Access
Data Transfer
Privacy Protection
Duration and Termination
Contact Information
Ethics Approval
Compensation
Liability
Publication Rights
Intellectual Property
Governing Law
Dispute Resolution
Amendment Provisions
Language Declaration
Voluntary Participation
Data Protection
Confidentiality
Purpose of Research
Research Procedures
Rights and Obligations
Risk Disclosure
Benefits
Withdrawal Rights
Data Storage and Security
Data Access
Data Transfer
Privacy Protection
Duration and Termination
Contact Information
Ethics Approval
Compensation
Liability
Publication Rights
Intellectual Property
Governing Law
Dispute Resolution
Amendment Provisions
Language Declaration
Relevant Industries
Academic Research
Healthcare
Pharmaceutical
Market Research
Social Sciences
Psychology
Medical Research
Education
Technology
Consumer Research
Clinical Trials
Relevant Teams
Legal
Research & Development
Compliance
Ethics
Data Protection
Clinical Operations
Academic Affairs
Research Administration
Quality Assurance
Regulatory Affairs
Relevant Roles
Research Director
Principal Investigator
Research Ethics Officer
Data Protection Officer
Legal Counsel
Research Coordinator
Clinical Research Manager
Academic Researcher
Research Administrator
Compliance Officer
Ethics Committee Member
Research Project Manager
Research Supervisor
Graduate Research Assistant
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