Essential requirements for those working with clinical trial samples.
This 30 min* narrated course is ideal for laboratory staff needing an insight into GCLP requirements, as well as sponsors’ monitors, medical experts and auditors who utilize laboratory services in clinical trials.
It is based on the guidance given in the European Medicines Agency “Reflection paper for laboratories that perform the analysis or evaluation of clinical trial samples”, adopted by the GCP Inspectors Working Group in 2012.
It covers the most important aspects in the Reflection Paper and offers practical advice on how and when a laboratory should comply.
The program also covers some GCP basics to fulfil the requirement that laboratory staff have relevant GCP knowledge.
Fantasic rates available for groups of 5 or more participants