FALLS CHURCH, Va., May 13, 2020 /PRNewswire-PRWeb/ -- Final ICH E6 (R2) Guideline on Good Clinical Practices The Real Impact of the Changes A CenterWatch Webinar ...

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 ...

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 ...

FALLS CHURCH, Va., April 21, 2020 /PRNewswire-PRWeb/ -- Get Ready for ICH E6(R3) How to Prepare When You're Still Struggling to Adopt ICH E6(R2) A Free CenterWatch Webinar, Sponsored by The Avoca ...

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 ...

PRINCETON, N.J., May 25, 2017 /PRNewswire/ -- At its annual Summit USA in New York City on May 10-11, 2017, the Avoca Quality Consortium (AQC) released a "Regulatory Roadmap" -- a set of practical ...

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 ...

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 ...

NEW YORK--(BUSINESS WIRE)--Sites, Sponsors and CROs are facing increased costs and regulations in the area of monitoring. For studies conducted by CROs alone, monitoring accounts for nearly 50% of the ...

CITI Program updates GCP curriculum and launches new course in response to ICH E6(R3) to support clinical trial compliance and training. Our updated GCP curriculum ensures that sponsors, investigators ...