***** ICH GCP E6 (R2) compliant *****
Bulk purchases qualify for special rates.
50-99 copies £6.95 each
100-249 copies £5.95 each
250-499 copies £4.95 each
500+ copies £3.95 each
Customisation is available at an additional cost on all orders over 100 copies.
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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.
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.
Translated by Valerie Dumon Jones & Guy Nickols.
This guide will help French reading members of the investigator site to comply with ICH GCP