DUBLIN--(BUSINESS WIRE)--The "The New ICH GCP E6 R2 Guideline" conference has been added to Research and Markets' offering With the new ICH GCP E6 Revision 2 changes now finalised and needing to be ...

For clinical trials, it's a whole new game. The ICH GCP E6 R2 guidelines now require sponsors/CROs to implement a CRO-vendor oversight framework… procedures ...

Sponsors of clinical trials can now easily perform an independent check of the data quality coming in from sites at any time, contribute to a risk-based approach to monitoring and check follow-up by ...

In November 2017, one of the EMA’s Inspectors, Sophia Mylona, reiterated the importance of Revision 2 (R2) to the attendees at the 5th Global QA conference in Edinburgh, Scotland. Her message ...

Edge Strategic Monitoring is Only RBM Solution to Address 95% of TransCelerate Technical Requirements and be Fully Compliant with ICH GCP E6 (R2) Requirements NEW YORK--(BUSINESS WIRE)--As clinical ...

In May 2023, the International Council for Harmonisation (ICH) released the third revision of the Good Clinical Practice E6 guidelines, replacing the E6 (R2) released in 2016. Currently, the document ...

Good Clinical Practice (GCP), the bedrock of ethical and high-quality clinical research, guides operations among sponsor companies, contract research organisations (CROs), investigator sites, and ...

In this free webinar, gain insight into the background and purpose of the ICH GCP E6(R3) updates. Attendees will learn about structural and content-based changes, including the top five most-impacted ...

The "Navigating ICH GCP (Good Clinical Practice) E6 (R3): What You Need to Know Training Course (Jan 29, 2026)" training has been added to ResearchAndMarkets.com's offering.