ICH E6(R3) Annex 2: Draft Version for Good Clinical Practice in Modern Clinical Trials
Draft ICH E6(R3) Annex 2 provides updated GCP guidelines for modern clinical trials, focusing on decentralized designs, data privacy, and participant safety.
Understanding GxP Regulations in The Pharmaceutical Industry
Navigate success in the pharmaceutical industry with GxP compliance. Explore GMP, GLP, GDP, and GCP for quality, safety, and regulatory excellence