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Clinical Trials Toolkit
Clinical Trials Toolkit provides practical advice to researchers designing and conducting publicly funded clinical trials in the UK. Through the use of an interactive routemap, it provides information on best practice and outlines the current legal and practical requirements for conducting clinical trials.
It’s primarily focused on Clinical Trials of Investigational Medicinal Products (CTIMPs) and the regulatory environment and requirements associated with these. However researchers and R&D staff working on trials in other areas will also find useful information and guidance of relevance to the wider trials environment.
Please note the Toolkit describes the requirements for Clinical Trials of Investigational Medicinal Products (CTIMPs) brought about by the introduction of the European Commission Directive 2001/20/EC. The site will consider the implications of any confirmed change in due course and provide updated information and guidance as agreed.
It’s primarily focused on Clinical Trials of Investigational Medicinal Products (CTIMPs) and the regulatory environment and requirements associated with these. However researchers and R&D staff working on trials in other areas will also find useful information and guidance of relevance to the wider trials environment.
Please note the Toolkit describes the requirements for Clinical Trials of Investigational Medicinal Products (CTIMPs) brought about by the introduction of the European Commission Directive 2001/20/EC. The site will consider the implications of any confirmed change in due course and provide updated information and guidance as agreed.
Resource details
| Contributed to: |
Community contributions Community resources are online learning and digital materials provided by the wider Learning Hub community that anyone can contribute to. |
| Contributed by: | Fatima Almeda |
| Authored by: |
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| Licence: | © All rights reserved More information on licences |
| First contributed: | 04 June 2013 |
| Audience access level: | Full user |
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