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Good Clinical Practice (GCP) is the internationally- recognized standard for the design, conduct, recording and reporting of clinical trials involving human subjects. Adherence to the principles of GCP is essential in ensuring ethical standards and scientific quality, while providing public assurance that the rights, safety and well-being of trial subjects are protected. This website focuses on the practical implementation of GCP standards, with an emphasis on training and development.



In-Person Seminars

Looking for instructor lead seminars covering process of pharmaceutical, device, and biotechnology product development?  Barnett International offers over 125 two or three day interactive, instructor lead seminars across the United States. 

Just some of the top seminars include:

Clinical Research
Drug Safety & Development
Medical Devices
Project Management

Click here to view a full listing of our upcoming seminars.

Barnett's On-Demand

Too busy to attend a course? Our newly- released GCP eLearning course may be your solution. For details on our scenario- based practical GCP application on- demand course, click here


2016 GCP Question & Answer Guide

Available in Hard Copy & Electronic Editions!  


July 2016 - January 2017 Edition Now Available  

-Download Today!