ICH GCP E6 (R2) 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.

All of our courses have been updated with ICH GCP Integrated Addendum E6 R2

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

Our online brochure can be found at


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ICH GCP Guidelines with Integrated Addendum E6 (R2) A5
This publication contains a uniquely indexed version of the ICH Harmonised Guideline entitled “Integ..
Interpreting Medical Records
by Dr Graham Hornett and Prof David Hutchinson A carry around pocketbook that contains hundreds o..
Key Requirements affecting Clinical Trials In Europe 5th Edition
This publication combines the key requirements and guidelines with a unique subject index that allow..
UK Clinical Trial Regulations, Indexed and Consolidated (3rd Edition)
This “Brookwood indexed” reproduction of the original Statutory Instrument 2004 No. 1031 also incorp..
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