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Short Consent Form For Research for Belgium

Short Consent Form For Research Template for Belgium

A legally compliant research consent form designed for use in Belgium, incorporating requirements from both Belgian national law and EU regulations (particularly GDPR). This document serves as a formal agreement between research institutions and study participants, ensuring informed consent while maintaining brevity and clarity. It includes essential information about the research study, participant rights, data protection measures, and withdrawal procedures, all structured to meet Belgian ethical research standards and language requirements.

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Short Consent Form For Research

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What is a Short Consent Form For Research?

The Short Consent Form For Research is a crucial document used in Belgian research settings to obtain and document informed consent from study participants. It is designed to comply with Belgian research laws, including the Law of 7 May 2004 concerning experiments on human persons, the Belgian Data Protection Act, and EU GDPR requirements. This document should be used whenever conducting research involving human participants in Belgium, whether in academic, clinical, or commercial settings. The form maintains brevity while ensuring all essential information is conveyed to participants, including study purpose, procedures, risks, benefits, and data protection measures. It must be available in the appropriate official language(s) of Belgium (Dutch, French, or German) depending on the region where the research is conducted.

What sections should be included in a Short Consent Form For Research?

1. Title and Header: Research study title, institution details, and document identification

2. Introduction: Brief introduction to the research study and purpose of the consent form

3. Study Purpose: Clear, non-technical explanation of the research objectives and why the study is being conducted

4. Participation Requirements: What participants will be asked to do, including time commitment and procedures

5. Risks and Benefits: Clear description of potential risks and benefits of participation

6. Data Protection and Privacy: How personal data will be collected, used, stored, and protected (GDPR compliance)

7. Voluntary Participation: Statement that participation is voluntary and can be withdrawn at any time

8. Contact Information: Details of researchers, ethics committee, and data protection officer

9. Declaration of Consent: Formal consent statement and signature blocks for participant and researcher

What sections are optional to include in a Short Consent Form For Research?

1. Compensation: Include when participants will receive payment or reimbursement for participation

2. Future Research Use: Include when collected data might be used for future research projects

3. Biological Samples: Include when the research involves collecting biological samples

4. Audio/Video Recording: Include when the research involves recording participants

5. Third Party Data Sharing: Include when data will be shared with other institutions or researchers

6. Commercial Development: Include when research might lead to commercial products or patents

What schedules should be included in a Short Consent Form For Research?

1. Detailed Study Procedures: Step-by-step description of study procedures and visits

2. Participant Information Sheet: More detailed information about the study in Q&A format

3. Data Processing Details: Detailed information about data processing activities and security measures

4. Withdrawal Form: Template form for participants to withdraw from the study

5. Glossary: Definitions of technical terms used in the consent form

Authors

Alex Denne

Head of Growth (Open Source Law) @ Genie AI | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

Jurisdiction

Belgium

Publisher

Genie AI

Document Type

Consent Form

Cost

Free to use
Relevant legal definitions
















Clauses



















Relevant Industries

Healthcare

Pharmaceuticals

Biotechnology

Academic Research

Clinical Research

Social Sciences

Psychology

Medical Devices

Educational Research

Market Research

Environmental Research

Agricultural Research

Relevant Teams

Legal

Research & Development

Clinical Operations

Regulatory Affairs

Compliance

Quality Assurance

Ethics Review Board

Data Protection

Research Administration

Clinical Research Unit

Relevant Roles

Research Director

Principal Investigator

Research Coordinator

Clinical Trial Manager

Ethics Committee Member

Data Protection Officer

Research Compliance Officer

Legal Counsel

Research Administrator

Study Nurse

Research Assistant

Quality Assurance Manager

Regulatory Affairs Specialist

Research Ethics Officer

Industries







Teams

Employer, Employee, Start Date, Job Title, Department, Location, Probationary Period, Notice Period, Salary, Overtime, Vacation Pay, Statutory Holidays, Benefits, Bonus, Expenses, Working Hours, Rest Breaks,  Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination,  Severance Pay, Governing Law, Entire Agreemen

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