How to Achieve An ISO 13485:2016 Compliant Quality System
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 Export to Your Calendar 8/29/2017
When: August 29, 2017
2pm ET
Where: United States
Contact: Sheri DeVinney
202-354-7171


Online registration is available until: 8/29/2017
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On Tuesday, August 29th, MDMA will present a member-only (no cost) webinar, How to Achieve An ISO 13485:2016 Compliant Quality System, hosted by IQMS Manufacturing ERP and MES and E.M.M.A. International Consulting Groups.

Dr. Carmine Jabri, President and CEO of E.M.M.A. International Consulting Group, Inc., will present an overview of the upgrades to ISO 13485:2016. E.M.M.A. International is a global leader in management consulting services, with headquarters in Farmington Hills, MI, as well as offices in FL & PA. They focus on quality, regulatory, and compliance services for the Medical Device industry.

 

Ed Potoczak, Director of Industry Relations of IQMS Manufacturing ERP and MES, will then discuss practical opportunities to apply proven, purpose-built software used by many medical device makers to drive real-time quality, traceability, accurate product identification, and efficiency in support of FDA compliant, best-in-class operations.