Webinar Recording: Regulatory Compliance for Medical Devices in Today’s new world
In Today’s world, Medical Device companies need an end-to-end solution supporting all aspects of a medical device company’s quality system and regulatory compliance ISO-regulated design controls.
High consumer expectations for better healthcare and advances in technology that improve quality of life are creating favorable market conditions for medical device companies. But increasing regulatory scrutiny is forcing medical device manufacturers to focus more on quality and safety. The License to Cure for Medical Device solution allows companies to eliminate scattered processes and data and to “embed” regulations as an asset, optimizing quality and compliance and reducing cost and time to market.
Join Michael McKittrick, Industry 4.0 evangelist with more than 20 years of experience in the Industrial Market and Dassault systemes Warren Perry, Industry Process expert has worked in the Life Sciences industry for over 25 years and has a wealth of experience gained from tenure with EXTEDO, a Regulatory Publishing solution provider, and CDC Solutions, where he was a Technical Account Manager, and Product Manager.
Webinar Recording: Regulatory Compliance for Medical Devices in Today’s new world
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Michael Mckittrick
Michael McKittrick is a Technology Success Manager with Persistent Systems, helping customers accelerate their journey to Industry 4.0 as a Manufacturing & Engineering technology advocate.
Michael relies on more than 14 years of experience in CAD, PLM, ALM, IoT, CE and CLM systems to ensure the manufacturers IT ecosystem is in total alignment with the needs of the departments, individuals and goals of the organization and support both individual KPI achievement as well as the company’s business goals.
Warren Perry
Warren Perry started with QUMAS, now a part of ENOVIA almost 20 years ago, and during this time he held various positions including Product Marketing Manager, Marketing Manager and Project Lead, and has always been heavily involved in Pre-Sales activities. Warren has worked in the Life Sciences industry for over 25 years and has a wealth of experience gained from tenure with EXTEDO, a Regulatory Publishing solution provider, and CDC Solutions, where he was a Technical Account Manager, and Product Manager.
His career started in Content and Records Management on the West Coast of the US where he spent 18 years with companies such as Dunn & Bradstreet, EDS and Anacomp, a division of General Dynamics. For the past 20 years he has specialized in regulated electronic content management and data normalization as well as regulatory publishing, working with major energy, retail, banking and Life Sciences companies.
Warren brings to ENOVIA years of experience working for software companies, and an understanding of global markets in GRC, Regulatory Publishing and EDMS systems, having worked with clients such as McDermott, Chevron, Takeda, Samsung, Roche, Bank of America, Boehringer Ingelheim, GlaxoSmithKline, Fidelity Investments, Logica CMG, and Aspen Pharmaceuticals.