❓ Do you want to understand the principles of the new version of ICH GCP E6 (R3)?
❓ Who has what roles and responsibilities in clinical research?
❓ How do the rules reflect digitization, data processing, and new technologies?
❓ What are the benefits of emphasizing quality and adopting a risk-based approach?
❓ How are the requirements for informed consent and transparency in clinical trials changing?
Clinical research is now more flexible and patient-friendly. The new version of ICH GCP E6 (R3), effective as of the 23rd, 7. 2025, which more clearly defines roles and emphasizes minimizing the burden on the patient.
CZECRIN Academy, in collaboration with experts from ASKAS—the Association of Study Coordinators and Nurses— the Association for Innovative Pharmaceutical Industry (AIFP), and ACRO CZ, has developed the first comprehensive course on this new version based on real-world experience—and it’s entirely in Czech!
Forget about hundreds of pages of technical English—we’ve prepared a commentary in Czech, added real-world examples, and turned it into a course that will truly save you time and stress.
What will you find in the course?
🔹 The complete text of ICH GCP E6 (R3)
🔹 Nine narrated videos (112 minutes)
🔹 Printable materials
🔹 A collection of useful links
🔹 Glossary
The course also includes a short test to assess your knowledge, upon completion of which you will receive a full certificate.