“Ensuring Market Access via Environment Compliance” webinar (includes AB Sciex case study)

From 08:00 July 27, 2015 to 12:00 August 01, 2017
On Demand

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.

Attend this webinar to learn:

  • The “Data Management Challenge” of determining and ensuring complete regulatory compliance of your products;
  • The business process and data flow enabled by the ENOVIA Material Compliance solution;
  • A unique approach from AB Sciex, a leading medical device manufacturer, who was able to better manage their compliance business risk after implementing the ENOVIA Materials Compliance Central™ solution as part of their overall PLM strategy.

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.

Registration form