Short Consent Form For Research

Short Consent Form For Research Template for England and Wales

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Key Requirements PROMPT example:

"I need a Short Consent Form For Research for a medical study on diabetes treatment effectiveness, to be conducted at Oxford University starting March 2025, which includes provisions for blood sample collection and data sharing with international research partners."

What is a Short Consent Form For Research?

The Short Consent Form For Research is a fundamental document required for any research involving human participants in England and Wales. It serves as a legal record of informed consent and is designed to protect both the participants' rights and the researchers' interests. The form must comply with UK GDPR, the Data Protection Act 2018, and various research governance frameworks. It typically includes essential information about the study, data handling procedures, participant rights, and researcher responsibilities. This document is particularly crucial for ensuring ethical research conduct and maintaining regulatory compliance across academic, medical, and social research sectors.

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

1. Study Title: Clear identification of the research project and version number

2. Principal Investigator Information: Name, institution, and contact details of the lead researcher and research team

3. Purpose of Research: Brief, clear explanation of research objectives in plain language

4. Participation Statement: Confirmation that participation is voluntary and can be withdrawn at any time

5. Data Protection Statement: Information about how personal data will be collected, stored, used and protected in compliance with UK GDPR

6. Signature Block: Space for participant name, signature, date, and researcher countersignature

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

1. Biological Samples Section: Details of sample collection, storage, and usage when research involves human tissue samples

2. Future Research Use: Optional consent for data or sample use in future research projects

3. Payment Information: Details of any compensation or reimbursement for participation

4. Audio/Video Recording: Specific consent for recording of interviews or procedures if applicable

5. Medical Records Access: Permission to access relevant medical records if required for the research

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

1. Participant Information Sheet: Detailed information about the study, risks, benefits, and participant rights

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

3. Contact Card: Emergency contact information for research team and relevant support services

4. Schedule of Procedures: Timeline and list of research procedures, visits, or interventions

Authors

Alex Denne

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

alex.den.21@genieai.co

Relevant legal definitions

Clauses

Relevant Industries

Healthcare
Academia
Pharmaceuticals
Psychology
Social Sciences

Relevant Teams

Research & Development
Legal
Ethics & Compliance
Data Protection
Clinical Operations

Relevant Roles

Research Director
Principal Investigator
Research Ethics Officer
Clinical Trial Manager
Research Coordinator

Find the exact document you need

Assent Form

A legal template under English and Welsh law used to obtain formal agreement from individuals who may not have full legal capacity to provide consent.

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Let's create your Short Consent Form For Research

What is a Short Consent Form For Research?

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

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

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

Authors

Alex Denne

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