The Clinical Trial Agreement Template UK is offered in multiple formats, including PDF, Word, and Google Docs, featuring customizable and printable examples.
Clinical Trial Agreement Template UK Editable – PrintableSample
Clinical Trial Agreement Template UK 1. Trial Sponsor Information 2. Investigator Information 3. Clinical Trial Details 4. Objective of the Trial 5. Scope of Work 6. Responsibilities of the Sponsor 7. Responsibilities of the Investigator 8. Compensation and Payment Terms 9. Confidentiality and Data Protection 10. Indemnity and Liability 11. Termination Conditions 12. Signatures and Agreement 13. Declaration and Signatures
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WORD
Examples
[Name of the Sponsor]
[Sponsor’s ID]
[Sponsor’s Address]
[Sponsor’s Phone]
[Sponsor’s Email]
[Name of the Investigator]
[Investigator’s ID]
[Investigator’s Address]
[Investigator’s Phone]
[Investigator’s Email]
This agreement defines the terms and conditions under which [Name of the Investigator] will conduct the clinical trial titled “[Trial Title]” commencing on [Start Date].
The primary objective of the study is to evaluate [Brief Description of Study Objectives].
The Investigator agrees to conduct the trial in accordance with applicable regulations, including GCP and any stipulations outlined in the protocol.
The Sponsor agrees to compensate the Investigator with a total payment of [Amount], disbursed according to the schedule defined in [Payment Schedule].
Both parties agree to maintain the confidentiality of all proprietary information and comply with applicable data protection laws.
The Sponsor shall provide adequate insurance coverage for the trial, ensuring liability coverage against injury or damage related to the study.
Either party may terminate this agreement with [Notice Period] written notice to the other party if there are breaches in contract conditions.
This agreement shall be governed by the laws of [Jurisdiction, e.g., England and Wales].
[Signature of the Sponsor]
[Name of the Sponsor]
[Signature of the Investigator]
[Name of the Investigator]
[Name of the Sponsor]
[Sponsor’s ID]
[Sponsor’s Address]
[Sponsor’s Phone]
[Sponsor’s Email]
[Name of the Investigator]
[Investigator’s ID]
[Investigator’s Address]
[Investigator’s Phone]
[Investigator’s Email]
This clinical trial agreement outlines the responsibilities and terms for the study titled “[Trial Title]”, effective from [Start Date].
The Investigator shall adhere strictly to the approved trial protocol and make necessary notifications in case of protocol amendments.
The Investigator agrees to maintain accurate records and reports of trial data, ensuring compliance with the relevant guidelines and standards.
Payments shall be made based on [Specify Payment Terms, e.g., milestones, patient enrollment, etc.].
The results of the trial may be published, subject to mutual agreement and with consideration of confidentiality aspects.
Both parties commit to comply with all applicable laws, including ethical standards and regulatory requirements for conducting clinical trials.
The Sponsor has the right to audit the study at reasonable times to ensure compliance with the study protocol and regulatory requirements.
This agreement shall be governed by the laws of [Jurisdiction, e.g., England and Wales].
[Signature of the Sponsor]
[Name of the Sponsor]
[Signature of the Investigator]
[Name of the Investigator]
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