A trial master file is a collection of important documents pertaining to a study, clinical trial or other form of research. Periodically, the trial master file must undergo audits to ensure the ...
In April 2017, the European Medicines Agency (EMA) issued a draft guideline (“Draft Guideline“) concerning the Trial Master Files (“TMF”) for public consultation. The Draft Guideline updates the ...
"Browse 230 market data Tables and 43 Figures spread through 300 Pages and in-depth TOC on "Electronic Trial Master File (eTMF) Systems Market by Offering (Integrated, Standalone), Function (Analytic, ...
The Global Electronic Trial Master File (eTMF) Systems market is expected to witness a growth rate of 12% by 2027. The growth in the number of clinical trials, a surge in the volume of data generated, ...
AMERSHAM, U.K., June 20, 2019 /PRNewswire-PRWeb/ -- Phlexglobal today announced an important industry advisory around the new European Medicines Agency (EMA) guidance on Trial Master Files. The ...
MALVERN, Pa. and AMERSHAM, United Kingdom, July 20, 2020 /PRNewswire-PRWeb/ -- A newly announced technical partnership between Arkivum, recognized internationally for its cross-sector expertise in ...
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