Medical device developers are operating under increasingly stringent regulations. The guide below examines why medical device manufacturers are increasingly turning to ERP systems to mitigate compliance risk and turn developmental concepts into commercialized product offerings with greater efficiency.
Breaking Barriers and Driving Change: A Conversation with Manda Pasarkar, Director of Global Regulatory Affairs, CMC at
In this Speaker Spotlight, Guillaume Blivet, Co-Founder & Chief Innovation Officer at REGEnLIFE, will give a preview of...
In this Speaker Spotlight, Jules Keghie, Ph.D., VP and Head of System Engineering and Architecture, Elekta, will give a...
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