Choose the license that fits your learning needs.
Learn everything you need to know to master the Sponsor responsibilities of ICH GCP for International Clinical trials
Learn about the setup and conduct of clinical trials with medical devices in Europe according to the MDR.
Our all inclusive EU CTR Expert course for clinical drug trials in Europe helps you understand all the vital aspects of the EU CTR regulation.
Master the new EU CTR regulation efficiently.
Learn everything you need to know to master the Site's responsibilities of ICH GCP for International Clinical trials.
Expert Online ICH GCP Course for International Clinical Trials
The ICH/GCP course is the perfect online training for research professionals working on international trials.
Learn the fundamental elements of the new EU CTR.
The EU CTR Foundation course gives you the fundamentals of the new EU CTR regulation.
Add this course to the Expert Online ICH GCP Course for International Clinical Trials
Learn about the principles the Code of Federal Regulations (CFR) add to the ICH-GCP expectations and get a detailed understanding of the knowledge required for clinical trials in the USA.
Learn about the principles of Good Manufacturing Practice (GMP), the legal requirements and best practices for effective and efficient Quality Oversight on external manufacturing. Consists of 3 interactive module containing 7 chapters.
Basic course on fundamental knowledge in clinical studies
Refresher course for study nurses and members of an investigational team in clinical trials according to the German Medicines Act, the AMG
Update course for nurses and members of a trial team in clinical trials under the Medicines Act (AMG) and Regulation (EU) No. 536/2014
Learn about the regulatory-ethical prerequisites for the conduct of clinical drug trials