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September 2019
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By Generis
CARA, Generis' innovative and leading user interface for Documentum now assists Medical Device Companies in meeting FDA and other regulatory and quality requirements for the design, development and manufacture of Medical Devices.
By Generis
Generis is pleased to announce the release of the updated CARA preconfigured module for Quality / SOP / GxP documentation, based on the DIA Reference Model.

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