ICH E6 (R2) GCP Training v2.0
This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, In
Enroll in Course
If an auditor, regulatory inspector or client asked for you to provide documentation of your GCP training compliance, could you?
Such a fundamental oversight of the most universal & basic requirement of study conduct brings to question the integrity of your hard work and efforts.
This is an easy, affordable and compliant solution.
A Good Clinical Practice (GCP) course ideal for busy people participating in the conduct of clinical research who require documented GCP training.
Format: Self-paced learning with an assessment to demonstrate your understanding of the material presented. Upon successful completion, a certificate will be issued for your records.
This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, Inc. as necessary to enable mutual recognition of GCP training among trial sponsors.
Your Instructor
An exceptionally experienced & respected legacy pharmaceutical colleague having held operational responsibility for some of the largest and most influential clinical trials in the world. Georg has organized and delivered training to thousands of research professionals around the world and looks forward to sharing his knowledge with you!