A US based global Biotech company, in order to streamline their processes was looking for a complete electronic trial master file (TMF) system built up. The immediate bottleneck was that there was no immediate access to client’s data to track progress on each study. As the client was in collaboration with the other CRO, there was difficulty in sticking to the existing structure and tracking consistency and credibility of the data.

Reading through this document, you will learn how Freyr built a centralized eTMF system as per industry standard specifications (DIA – RM V3)

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