Balancing high quality with achieving global regulatory compliance are a constant challenge for medical device manufacturers. The consequences of focusing on just one versus the other causes various problems including: cost overruns, strained customer relations and market entry delays which leads to loss of market share. The ENOVIA Materials Compliance solution helps companies manage these competing requirements in a single, collaborative environment that helps connect multiple processes and information from quality, regulatory, engineering and the supply chain.
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Fill out the form below to register to attend this webinar delivered by Mike Zepp from Dassault Systèmes and Mr. George Valaitis from AB Sciex.