Clinical Research:  The Principles of Good Clinical Practice

This 2 Day workshop would set the foundations on understanding the requirements of ICH GCP and on how to successfully conduct a clinical trial, ensuring the safety, rights, well being of the trial subjects are protected and the data that is produced from the clinical trial is complete accurate and unbiased.  

This workshop is applicable to all Investigators, Sub Investigators, Study Coordinators and other relevant site staff.

NOTE:  This ICH E6 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.​