The requirements in the field of clinical trial monitoring have increased. In addition to a sound knowledge of the German Medicines Act (AMG), the German Regulation on Good Clinical Practice (GCP-V) and EU legislation, continuous training and special knowledge in handling the electronic systems used are also required.
In order to deepen his knowledge in this field, one of ClinTriCare’s Project Coordinators will participate in the seminar “Monitoring of Clinical Trials on Drugs” on 15/16 October 2014 in Heidelberg. Particularly the exchange with the fellow attendees and the sharing of useful tips by the experts round off such an advanced training course.
The program is available online at www.akademie-heidelberg.de.