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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.
The MDR course is the perfect solution for research professionals involved in clinical trials with medical devices in Europe, and need to know about the changes due 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.
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 everything you need to know to master the Sponsor responsibilities of ICH GCP for International Clinical trials
Learn everything you need to know to master the Sponsor responsibilities of ICH GCP for International Clinical trials.
Learn everything you need to know to master the Site's responsibilities of ICH GCP for International Clinical trials.
Learn about the principles of Gooad 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.
Fundamental ICH GCP Course to Start and Conduct International Clinical Trials
The right choice for people contributing to some activities in global clinical research but don't need to know every detail of GCP (yet)
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 the fundamental elements of the new EU CTR.
The EU CTR Foundation course gives you the fundamentals of the new EU CTR regulation.
Our EU CTR Reviewers e-learning course not only helps you understand the upcoming EU CTR regulation, but offers a clear and in-depth understanding.
Get EU CTR fundamentals and master reviewing dossiers according to the new EU CTR procedures.
Our EU CTR Conduct e-learning course gives you the essentials on the upcoming EU CTR regulation, as well as an in-depth understanding
Deep dive into preparing and submitting submission packages with our fundamental EU CTR Submission e-learning course.
Get EU CTR fundamentals and master preparing, and submitting dossiers.
Introductory ICH GCP Course to Design International Clinical Trials
The light ICH/GCP course is ideal for research staff who contribute to international clinical trials, but do not need to know every detail of GCP.
Introductory ICH GCP Course to Prepare International Clinical Trials
Introductory ICH GCP Course to Submit International Clinical Trials
Introductory ICH GCP Course to Start International Clinical Trials
Introductory ICH GCP Course to Conduct International Clinical Trials
Introductory ICH GCP Course to Close International Clinical Trials
Basic ICH GCP Test for International Clinical Trials
The GCP Test is an excellent way to test your GCP knowledge and expand your knowledge with the rich feedback you receive after completion of the test.