Our course provides you with a summary of the current regulatory, ethical and methodological requirements for the conduct of clinical drug trials in Germany and Europe.

It can be booked as a stand-alone course or as the first module of a "blended" basic course for investigators according to the German Curriculum of the Bundesärztekammer (only in German).

You can learn with our approximately three-hour, interactive course on your smartphone, tablet or PC in self-selected pace. A modular structure and division into content chapters enables an individual learning experience. From registration onwards you will have 4 weeks to complete the course. After successfully completing a final knowledge test, you will receive a certificate from the Forschungsdock Akademie.

Who is this course for?  

For employees of sponsors, CROs or freelancers, our course provides a condensed summary of the currently valid ethical (Module 1) and regulatory (Module 2) prerequisites for clinical trials with medicinal products. Methodological essentials for drug studies (module 3) including risk management are also covered.

For investigators who want to work on clinical trials, our course represents the first part of the GCP Basic Course. Supplemented with a three-hour virtual classroom training, the course meets the requirements of the curricular training of the German Medical Association. The virtual classroom training is only available in German and can be booked via https://www.forschungsdock.de/praesenzseminare/.