Persons who are involved in conducting Clinical trials are required to have up to date training in ICH-Good Clinical Practice (GCP). This online training module is aimed at Investigators and site staff including research nurses, research fellows and research assistants.

This course is given by a clinical research regulatory director who has over 20 years CT experience. The course covers:

• 13 Principles of ICH-GCP  
• Current regulation of CTs in EEA,
• Investigator Responsibilities.   

This 4-hour online course can be taken at users own pace over 4 weeks.

Attendees will receive a certificate of attendance which is valid for 2 years.

This course 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.

Important: If you are UCC Staff please contact cpd@ucc.ie for CRFC Staff Fee Concession