Posted on: September 17-2018 | By : Sagar Mahajan | In: Life Sciences,Pharmaceuticals and Biotech | 1 Comment
Traditionally, a trial master file (TMF) has been thought of as a collection of documents to be collated to satisfy the regulatory requirements of a clinical study. While this is still the case, today’s increasing use of electronic TMFs and integrated clinical systems is giving the industry a more holistic and real-time view of clinical trial activities.

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Sagar Mahajan
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