UCC CPD courses

ICH-Good Clinical Practice for Investigators and Site staff


Fact File


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.


Fees and Costs


How Do I Apply

Applications can be made via link below:

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