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Clinical Research Associate (CRA) Training
This course goes through the whole clinical trial process and also includes aspects of Good Clinical Practice and Good Documentation Practice/Essential Documents.
Clinical Trials Audit Preparation
The course describes what investigational medicinal product sponsors, contract research organisations and clinical investigators can expect when they undergo inspection or audit.
GCP Refresher
This is a professionally developed training course which incorporates the ICH E6 R2 update implemented in June 2017, along with the new EU Clinical Trials Regulation which became live on the 31st January 2022.