Understanding ICH GCP E6 (R3): A New Era for Clinical Trials
In the ever-evolving landscape of clinical research, staying up to date with regulatory guidelines is crucial for ensuring patient safety and data integrity. The recent release of the International Council for Harmonisation’s (ICH) Good Clinical Practice (GCP) E6 (R3) guideline marks a significant milestone in the field. This third revision of the internationally recognized standard is set to reshape the entire clinical trial lifecycle, from design and conduct to monitoring, recording, and reporting. As we approach the implementation date of July 23, 2025, it’s essential for all stakeholders in the clinical research industry to understand the key changes and their implications. This blog post aims to provide a comprehensive overview […]
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