Good Clinical Practice is the backbone of ethical, credible clinical trials. It protects participant rights and safety while ensuring trial data is reliable, verifiable, and scientifically sound. GCP is not optional guidance. It is the standard that regulators expect sponsors, investigators, and monitors to follow across every phase of research. This article explains what GCP actually does in practice by: • Defining responsibilities across sponsors, investigators, and monitors • Establishing doc
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The Principles of GCP in Research A short animation on the principles of Good Clinical Practice in Research. Including delegation of duties amongst research staff, where to find training, essential documentation and informed consent. Created by the Research & Development Team at Cumbria, Northumberland, Tyne & Wear NHS Foundation Trust (CNTW). Watch the animation to learn more: | Sci Ani
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