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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Essential GCP for Investigators - German
Online GCP Training with German narration                ..
Essential GCP for Investigators - Hungarian
Online GCP Training in Hungarian (read-only)        In order to get your CDP ..
Essential GCP for Investigators - Italian
Online GCP training with Italian narration                ..
Essential GCP for Investigators - Japanese
Online GCP Training with Japanese narration                ..
Essential GCP for Investigators - Latin American Spanish
Online GCP Training  with Latin American Spanish narration          ..
Essential GCP for Investigators - Polish
Online GCP Training with Polish narration                ..
Essential GCP for Investigators - Russian
Online GCP Training with Russian narration               ..
Essential GCP for Investigators - Serbian
Online GCP Training in Serbian (read-only)                ..
Essential GCP for Investigators - Turkish
Online GCP training with Turkish narration                ..
e-book ICH GCP Guidelines with Integrated Addendum E6 (R2)
A uniquely indexed copy of the ICH GCP guidelines.             ..
e-book European Clinical Trial Regulation No. 536/2014
A uniquely indexed copy of the European Clinical Trial Regulation.         ..
e-book Key Requirements affecting Clinical Trials In Europe 5th Edition
A uniquely indexed and cross-referenced ICH GCP, EU GCP Directives, Helsinki and more.   ..
e-book Essential GCP Book
An easy to read overview of GCP.                   ..
e-book 12 Golden GCP Rules for Investigators
A concise summary of GCP responsibilities in numerous languages.         ..
e-book 15 Golden IND/GCP Rules for Investigators
Take 12 GCP Rules and add 3 IND rules for investigators doing US IND trials.      ..
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