GCP

GCP

ICH GCP E6 (R3) training for sponsors, investigators, regulators and others in 14 languages

Our GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors.


ICH Good Clinical Practice (GCP) is the widely used international ethical, scientific and practical standard to which all clinical research is conducted. Compliance with GCP provides public assurance that the rights, safety and wellbeing of human research participants are protected and that research data are reliable.
Everyone involved in the conduct of clinical research must be competent to perform their tasks, qualified by education, training and experience.
Our training courses address the GCP aspects of this requirement.

We are currently in the process of updating our courses to be ICH GCP (E6(R3) compliant. Please check with us to ensure we fulfil your requirements.

Contact us for fantastic group rates for 5 or more participants on any course

Our online brochure can be found at https://brookwood-global.com/Books/Online-Training-Brochure/


 


European Clinical Trial Regulation No. 536/2014 (A5)

European Clinical Trial Regulation No. 536/2014 (A5)

A uniquely indexed reproduction of the European Clinical Trial Regulation 2014  No. 536 as pub..

£19.95

12 Golden GCP Rules for Investigators

12 Golden GCP Rules for Investigators

Every investigator should have a copy of this book! It is an easy-to-read guide for investigator sit..

£9.95

14 Golden IND/GCP Rules for Investigators

14 Golden IND/GCP Rules for Investigators

This quick and easy to read, illustrated, bullet-point guide breaks down IND requirements and ICH GC..

£9.95

Interpreting Medical Records

Interpreting Medical Records

by Dr Graham Hornett and Prof David Hutchinson A carry around pocketbook that contains hundreds o..

£8.95

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