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The Montrium Blog

The most helpful and thought-provoking ClinOps content from our writers on the front-lines of the life sciences industry

Trial Master Files (TMFs) represent a significant challenge for pharmaceutical organizations in today’s clinical trial environment. The sheer volume of artifacts and documentation that is required to be created and managed throughout a clinical trial often makes compiling a TMF a lengthy, time-consuming and cumbersome task. Couple this with the distributed and global nature of clinical studies, and you’ve got an arduous and intensely manual job on your hands.

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