Researchers should be appropriately trained and qualified for their activities within a research study.
We have issued guidance regarding the requirements for researchers to undertake training.
Good Clinical Practice
Good clinical practice (ICH-GCP) is a set of internationally recognised ethical and scientific quality requirements that must be followed when designing, conducting, recording and reporting Clinical Trials of Investigational Medicinal Products (CTIMPs).
Please visit our dedicated ICH-GCP webpage for more information and to also read our joint statement with the MHRA, which explains when it is appropriate to follow ICH-GCP.