RIMs "By the Numbers" A Quick Look Guide to Inproving Your Global Submissions by Alex Butler

November 16, 2018

Different countries enforce a diversity of medical device regulations and standards. For regulatory affairs (RA) professionals responsible for global registrations, this means that submissions processes for devices become exponentially more problematic with each new market that is targeted. 

In this video, MasterControl Medical Device Solutions Manager Alex Butler provides useful project management statistics and shares helpful strategies for simplifying global submissions to ensure timely medical device registrations and , ultimately, get products to market sooner. Drastic global regulatory changes are on the horizon, so there’s no better time to prepare for the impending regulatory information management storm and learn how to target new markets.

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