eLearning on the Code of Federal Regulations (CFR)

Familiarize yourself with the principles that the Code of Federal Regulations (CFR) add to the ICH-GCP expectations. Get a detailed understanding of the knowledge required for clinical trials in the USA.

Our CFR online course for clinical research in the USA is ideal for individuals involved in the design, conduct, oversight, or management of clinical trials with drugs or biologics in the USA, who need to learn about the additional requirements by the FDA. This could be employees of Clinical Research Organizations (CROs) or Sponsor companies as well as Investigators, Research Nurses, and Clinical Research Coordinators.

The course consists of 1 module with 7 chapters and includes expert interviews and practical case scenarios as well as handy tools for your work and will serve as an addition to your ICH-GCP knowledge.

eLearning on smartphone, tablet or PC in self-selected stages!

Our interactive course can be started, interrupted and resumed anytime, anywhere. Learn at your own pace! Please note that this e-learning is only available in English.

Who is this course for?

• For employees of sponsors and CROs as well as freelancers
• For investigators, research/study nurses and clinical research coordinators