The world of clinical research is evolving — and so are the standards that govern it.
If you’re working in clinical trials, regulatory affairs, or quality assurance, understanding the ICH E6 Good Clinical Practice (GCP) guidelines is essential.
With the R3 revision emphasizing risk-based quality management, digital data integrity, and decentralized trials, now is the perfect time to upskill and stay compliant.
Here’s how you can get certified in ICH E6 (R2/R3) in 2025:
1️⃣ Choose a recognized training provider — Look for accredited institutions (e.g., TransCelerate, DIA, Coursera, or accredited GCP academies).
2️⃣ Complete the ICH E6 course modules — Covering R2 fundamentals and R3 updates (risk management, sponsor responsibilities, data integrity).
3️⃣ Pass the final assessment — Most programs include a quiz or case-based evaluation to test your GCP understanding.
4️⃣ Earn your certificate — Valid proof of GCP compliance and competency.
5️⃣ Keep it current — With R3 still in adoption, continuous learning is key.

Pro tip: If you’re already certified in R2, an R3 bridging course can help you transition smoothly to the updated standard.
Staying ahead in GCP means embracing change — and R3 is setting the stage for smarter, more transparent, and technology-driven clinical trials.