The Consent Form For Research is a crucial document required for any research involving human subjects in Hong Kong. It serves as a legal and ethical safeguard, ensuring that research participants are fully informed about the study's purpose, procedures, risks, and benefits before giving their consent. The document must comply with Hong Kong's Personal Data (Privacy) Ordinance, research ethics guidelines, and relevant institutional requirements. It is essential for both academic and commercial research, particularly in medical, social science, and behavioral studies. The form should be used whenever conducting research involving human participants, whether in educational institutions, healthcare settings, or corporate environments, and must be approved by relevant ethics committees before implementation.
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1. Title and Header: Research study title, institution details, and form identification
2. Introduction: Brief overview of the research study and purpose of the consent form
3. Researcher Information: Names and contact details of principal investigator and research team
4. Study Purpose: Clear explanation of research objectives and importance
5. Participation Requirements: Details of what participation involves, including time commitment and procedures
6. Risks and Benefits: Clear explanation of potential risks and benefits of participation
7. Confidentiality and Data Protection: Information about how personal data will be collected, stored, used, and protected
8. Voluntary Participation: Statement about voluntary nature of participation and right to withdraw
9. Costs and Compensation: Information about any costs or compensation related to participation
10. Contact Information: Details for questions, concerns, or complaints
11. Declaration and Signatures: Confirmation of understanding and consent by participant and researcher
1. Medical Procedures: Required when research involves medical tests or procedures
2. Audio/Video Recording Consent: Required when research involves recording of participants
3. Future Research Use: Optional section for consent to use data in future research
4. Translator Declaration: Required when consent form is explained through a translator
5. Parent/Guardian Consent: Required for research involving minors or individuals unable to provide consent
6. Witness Statement: Required when participant is illiterate or unable to read consent form
7. Commercial Use Declaration: Required when research may lead to commercial products
1. Detailed Research Protocol: Complete description of research procedures and methodology
2. Privacy Policy: Detailed information about data protection and privacy measures
3. Participant Information Sheet: Detailed information about the study in lay language
4. Risk Assessment Form: Detailed assessment of potential risks and mitigation measures
5. Contact Details: Complete list of research team and relevant institutional contacts
6. Withdrawal Form: Template form for participants to withdraw from the study
Relevant legal definitions
Research Study
Principal Investigator
Research Team
Participant
Personal Data
Sensitive Personal Data
Research Protocol
Ethics Committee
Informed Consent
Confidentiality
Data Protection
Research Institution
Study Procedures
Withdrawal Rights
Compensation
Adverse Event
Research Materials
Data Processing
Anonymous Data
Pseudonymized Data
Study Period
Research Records
Legal Representative
Sponsoring Organization
Research Site
Data Storage
Data Retention Period
Research Purpose
Third Party
Vulnerable Person
Consent Withdrawal
Research Results
Publication Rights
Secondary Use
Principal Investigator
Research Team
Participant
Personal Data
Sensitive Personal Data
Research Protocol
Ethics Committee
Informed Consent
Confidentiality
Data Protection
Research Institution
Study Procedures
Withdrawal Rights
Compensation
Adverse Event
Research Materials
Data Processing
Anonymous Data
Pseudonymized Data
Study Period
Research Records
Legal Representative
Sponsoring Organization
Research Site
Data Storage
Data Retention Period
Research Purpose
Third Party
Vulnerable Person
Consent Withdrawal
Research Results
Publication Rights
Secondary Use
Clauses
Voluntary Participation
Research Purpose
Study Procedures
Data Protection
Confidentiality
Privacy Rights
Risk Disclosure
Benefits
Compensation
Withdrawal Rights
Emergency Procedures
Record Keeping
Publication Rights
Data Access
Information Sharing
Liability
Medical Care
Translation Rights
Future Research Use
Commercial Rights
Intellectual Property
Contact Information
Complaint Procedures
Ethics Approval
Consent Declaration
Termination Rights
Amendment Procedures
Governing Law
Witness Requirements
Declaration of Understanding
Research Purpose
Study Procedures
Data Protection
Confidentiality
Privacy Rights
Risk Disclosure
Benefits
Compensation
Withdrawal Rights
Emergency Procedures
Record Keeping
Publication Rights
Data Access
Information Sharing
Liability
Medical Care
Translation Rights
Future Research Use
Commercial Rights
Intellectual Property
Contact Information
Complaint Procedures
Ethics Approval
Consent Declaration
Termination Rights
Amendment Procedures
Governing Law
Witness Requirements
Declaration of Understanding
Relevant Industries
Healthcare & Medical
Education & Academia
Pharmaceutical
Psychology & Behavioral Sciences
Social Sciences
Market Research
Technology & Innovation
Clinical Research
Biotechnology
Public Health
Relevant Teams
Research & Development
Legal & Compliance
Ethics & Governance
Clinical Operations
Data Protection
Academic Affairs
Medical Affairs
Regulatory Affairs
Human Resources
Quality Assurance
Relevant Roles
Research Director
Principal Investigator
Research Coordinator
Ethics Committee Member
Data Protection Officer
Clinical Trial Manager
Research Administrator
Legal Counsel
Compliance Officer
Research Ethics Officer
Academic Researcher
Research Assistant
Medical Director
Study Coordinator
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