Full course description
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 email@example.com for CRFC Staff Fee Concession