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 ...
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 ...
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 ...
There is no regulatory requirement that the research staff/person, who discovers or reports the adverse event be on the delegation log. The discovery of an AE can come from many sources - the subject, ...
Dublin, Nov. 03, 2025 (GLOBE NEWSWIRE) -- The "Navigating ICH GCP (Good Clinical Practice) E6 (R3): What You Need to Know Training Course (Jan 29, 2026)" training has been added to ...
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 ...
(MENAFN- GlobeNewsWire - Nasdaq) The ICH GCP E6 (R3) guideline presents market opportunities in training clinical research professionals for enhanced compliance. The focus is on integrating flexible, ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results