Managing Your Medical Device Master Files and Records

Whitepaper | March, 2018

In today’s age of Globalization and cut-throat competition, it has become competitive necessity for Manufacturers to leverage teams that located across geographies – you may have your design team in the US, your engineering team in India, your manufacturing team in China, and quality team in Germany. With such a geographically dispersed team, with each creating and storing their own set of files with different information, it has become increasingly difficult to find right information at the right time.

On the other hand, increased regulatory pressure, especially on regulated industries, has mandated organizations to ensure compliance with a set of standards or regulations – key to which is having well documented, objective evidence. This means organizations must have the ability to access all key data elements that are captured within different processes and link them not only to particular documents but also to specific and relevant sections within those documents.

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