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Learn everything you need to know to master the Sponsor responsibilities of ICH GCP for International Clinical trials.
Explore the biggest changes in the Good Clinical Practices revision from R2 to R3 and it’s impact on your clinical trial
Learn everything you need to know to master the Site's responsibilities of ICH GCP for International Clinical trials.
Learn about the principles of Good Manufacturing Practice (GMP), the legal requirements and best practices.
Learn about the setup and conduct of clinical trials with medical devices in Europe according to the MDR.
Learn about the principles the Code of Federal Regulations (CFR) add to the ICH GCP expectations.
Our all inclusive EU CTR training helps you understand all the vital aspects of the EU CTR regulation.
Our EU CTR Conduct e-learning course gives you the essentials on the EU CTR regulation, as well as an in-depth understanding.