The Short Consent Form For Research is a essential document required for any research involving human participants in the United Arab Emirates. It must comply with UAE Federal Law No. 4 of 2016 (Medical Liability Law) and other relevant research regulations. This document is used when researchers need to obtain informed consent from study participants, ensuring they understand the research purpose, procedures, risks, and benefits. The form should be written in clear, accessible language while maintaining all legally required elements. It's particularly important in the UAE context to consider cultural sensitivities and local ethical guidelines. The document must be available in Arabic and any other languages necessary for participant understanding, with certified translations where required.
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1. Study Title and Research Team: Clear identification of the research project and responsible investigators
2. Purpose of the Study: Brief, clear explanation of research objectives in lay terms
3. Participation Requirements: What participants will be asked to do and time commitment required
4. Risks and Discomforts: Clear outline of potential risks or inconveniences
5. Benefits: Description of direct benefits (if any) and broader scientific benefits
6. Confidentiality: How personal information and data will be protected
7. Voluntary Participation: Statement that participation is voluntary and can be withdrawn
8. Contact Information: Details for research team and ethics committee contacts
9. Participant Declaration: Confirmation of understanding and consent
10. Signatures: Space for participant and researcher signatures with dates
1. Compensation: Details of any payment or reimbursement, included when participants will receive compensation
2. Alternative Procedures: Description of alternative options, included for medical research
3. Future Use of Data: Information about data retention and future research use, included when data may be used beyond current study
4. Translation Declaration: Confirmation of accurate translation, included when form is provided in multiple languages
5. Witness Statement: Space for witness signature, included when required by vulnerability of participant or local requirements
6. Audio/Video Recording Consent: Specific consent for recording, included when study involves recordings
7. Biological Samples: Specific consent for collection and storage of biological samples, included in medical research
1. Detailed Study Procedures: Step-by-step description of research procedures
2. Participant Information Sheet: Detailed information about the study in Q&A format
3. Emergency Contact Protocol: Procedures and contacts for emergencies
4. Rights and Responsibilities: Detailed outline of participant rights and responsibilities
5. Data Protection Statement: Detailed information about data handling and protection measures
6. Withdrawal Procedures: Detailed process for withdrawing from the study
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Relevant Teams
Research and Development
Clinical Operations
Regulatory Affairs
Legal
Ethics Committee
Quality Assurance
Data Protection
Research Administration
Clinical Research
Medical Affairs
Compliance
Research Ethics
Relevant Roles
Research Director
Principal Investigator
Research Coordinator
Ethics Committee Chair
Clinical Trial Manager
Research Compliance Officer
Medical Director
Research Administrator
Data Protection Officer
Quality Assurance Manager
Research Ethics Officer
Study Site Manager
Research Project Manager
Regulatory Affairs Specialist
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