ICH GCP E6 (R2) training for sponsors, investigators, regulators and others in 11 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