Survey Consent Form for Malta
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Survey Consent Form
"I need a Survey Consent Form for a medical research study starting in March 2025, involving collection of sensitive health data from elderly participants in Malta, with specific provisions for audio recording interviews and potential data sharing with EU research partners."
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You keep IP ownership of your information
1. Introduction: Identifies the research organization, researchers, and basic purpose of the survey
2. Purpose of the Study: Detailed explanation of research objectives and potential benefits
3. Survey Procedure: What participation involves, including time commitment and type of questions
4. Data Collection and Processing: Information about what data will be collected and how it will be used
5. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time
6. Risks and Benefits: Description of any potential risks and benefits of participation
7. Confidentiality and Data Protection: How personal data will be protected, stored, and processed in compliance with GDPR
8. Participant Rights: Explanation of rights under GDPR and local law, including right to withdraw
9. Contact Information: Details of researchers, data protection officer, and relevant authorities
10. Declaration of Consent: Formal consent statement and signature section
1. Audio/Video Recording Consent: Additional consent section when surveys include audio or video recording
2. Sensitive Data Processing: Special section when collecting sensitive personal data as defined by GDPR
3. Third Party Data Sharing: Section required when data will be shared with third parties or other researchers
4. International Data Transfers: Required when data will be transferred outside the EU/EEA
5. Future Research Use: Optional consent for using data in future research projects
6. Compensation Information: Details about any compensation or incentives for participation
7. Parental/Guardian Consent: Required when participants are minors or vulnerable adults
1. Detailed Research Protocol: Comprehensive description of the research methodology and procedures
2. Data Protection Impact Assessment Summary: Summary of DPIA findings relevant to participants
3. Privacy Notice: Detailed privacy notice as required by GDPR Article 13/14
4. Withdrawal Form: Template form for withdrawing consent
5. Contact Details Sheet: Comprehensive list of all relevant contact information
Authors
Processing
Data Controller
Data Processor
Consent
Research Organization
Survey
Participant
Sensitive Personal Data
Data Protection Officer
Research Purpose
Anonymization
Pseudonymization
Data Subject Rights
Third Party
Data Transfer
Research Ethics Committee
Withdrawal of Consent
Data Retention Period
Research Protocol
Confidential Information
Data Security Measures
Legal Guardian
Research Findings
Data Storage
Data Collection
Data Protection
Confidentiality
Consent
Withdrawal Rights
Information Use
Risk Assessment
Participant Rights
Data Storage
Data Sharing
Research Purpose
Privacy Protection
Data Security
Participant Compensation
Contact Information
Complaint Procedures
Documentation
Third Party Access
Data Retention
International Transfer
Research Ethics
Liability
Amendment
Termination
Academic Research
Market Research
Healthcare
Social Sciences
Education
Public Policy
Corporate Research & Development
Consumer Products
Financial Services
Technology
Pharmaceutical
Non-Profit
Legal
Compliance
Research & Development
Data Protection
Ethics
Research Operations
Clinical Research
Market Research
Academic Affairs
Regulatory Affairs
Information Security
Privacy
Research Director
Data Protection Officer
Research Ethics Officer
Principal Investigator
Research Coordinator
Legal Counsel
Compliance Manager
Research Administrator
Privacy Officer
Research Project Manager
Survey Methodologist
Research Ethics Committee Member
Data Protection Specialist
Research Compliance Officer
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