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******* All versions are ICH GCP E6 (R2) compliant ***********
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by Prof David Hutchinson
Good Clinical Practice (GCP) is a global quality process that is applied to the conduct of all clinical trials on new medicinal products. Study investigators, including physicians and other healthcare professionals at all levels of experience, have GCP responsibilities, but most researchers do not full understand what this involves. Investigators who do not work in accordance with GCP will be unable to perform trials on new products in the future.
Customer Reading One of Our Publications
This quick and easy to read, illustrated, 'bullet point' guide to ICH GCP is ideal for investigators and other members of the study team.
This popular book will help investigators comply with ICH GCP investigator responsibilities and items on the monitor's wish list. The book contains relevant extracts from the guidelines.
All translations from the original English version have been undertaken by experienced clinical research personnel, working with GCP and QA in a pharmaceutical company setting.
This guide will help English reading members of the investigator site to comply with ICH GCP