The Consent Agreement Template UK is offered in multiple formats, including PDF, Word, and Google Docs, featuring editable and printable samples for your convenience.
Consent Agreement Template UK Editable – PrintableSample
Consent Agreement Template UK 1. Participant Information 2. Research Study Information 3. Purpose of the Study 4. Participation Details 5. Risks and Benefits 6. Confidentiality 7. Voluntary Participation 8. Contact Information 9. Consent Statement 10. Declaration and Signatures
PDF
WORD
Examples
[Name of the Participant]
[Participant’s ID]
[Participant’s Address]
[Participant’s Phone]
[Participant’s Email]
[Name of the Organization]
[Organization’s ID]
[Organization’s Address]
[Organization’s Phone]
[Organization’s Email]
This Consent Agreement outlines the terms under which [Name of the Organization] obtains informed consent from [Name of the Participant] for participation in [Description of the Activity, e.g., research study, data collection].
The purpose of this consent is to ensure that the Participant is fully informed about the nature, risks, and benefits of participating in [Description of the Activity].
The Participant will be involved in [Detailed Description of the Activity, including duration, procedures, and location].
The potential risks include [List potential risks], while the expected benefits include [List potential benefits].
The Organization will take all necessary steps to ensure the confidentiality of the Participant’s data in compliance with GDPR and other relevant regulations.
Participation is voluntary, and the Participant has the right to withdraw at any time without any consequence.
By signing below, the Participant acknowledges that they have read and understood the contents of this agreement and agree to participate under the outlined conditions.
[Signature of the Participant]
[Name of the Participant]
[Signature of the Organization Representative]
[Name of the Organization Representative]
[Name of the Participant]
[Participant’s ID]
[Participant’s Address]
[Participant’s Phone]
[Participant’s Email]
[Name of the Organization]
[Organization’s ID]
[Organization’s Address]
[Organization’s Phone]
[Organization’s Email]
This Consent Agreement provides a framework for obtaining informed consent from [Name of the Participant] to participate in [Description of the Activity, e.g., clinical trial, focus group].
The purpose of this agreement is to inform the Participant of their rights and the nature of the activity involved.
The Participant agrees to take part in [Detailed Scope of Participation, including types of data collected and duration].
The Organization commits to carrying out this activity ethically and transparently, ensuring the Participant’s rights are upheld.
All personal data will be handled according to the Data Protection Act 2018 and GDPR regulations to ensure the Participant’s privacy.
The Participant maintains the right to withdraw consent and discontinue participation at any time without penalty.
By signing this agreement, the Participant confirms that they understand the information provided and consent to participate.
[Signature of the Participant]
[Name of the Participant]
[Signature of the Organization Representative]
[Name of the Organization Representative]
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