The Quality and Regulatory Department of the Clinical Research Facility-Cork at the HRB-Clinical Research Facility, UCC will be running ICH-GCP training courses throughout 2016/2017. The course includes a brief introduction to the Drug Development Process, Principles of ICH-GCP, Investigator Responsibilities and Essential Documents. The course has been developed and will be delivered by CRF-C Quality and Regulatory Affairs Manager, Dr. Ruben Keane and CRF-C Monitor Ms. Maire McCarthy.
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. The course also has Category 1 approval from An Bord Alternais and Registered Nurses and Midwives who attend will receive 3.5 CUEs. Physicians who attend the half-day course are eligible for 3 Continuing Professional Development (CPD) points from the Royal College of Physicians in Ireland (RCPI).
Participants will receive a certificate of attendance following the course, this is valid for 2 years.
|6th December 2016||09.30-13.00|
|15th February 2017||09.30-13.00|
|10th April 2017||13.30-17.00|
|12th June 2017||09.30-13.00|
|12th September 2017||09.30-13.00|
|16th November 2017||13.30-17.00|
If you would like to reserve a place on the course or if you have any further queries please do not hesitate to contact us at email@example.com.