Jay Crowley, Grant Hodgkins to Present at the MDR & IVDR EU Conference 2017 in Orlando, Florida for USDM Life Sciences

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I am looking forward to facilitating some critical discussions surrounding the MDR and IVDR requirements and sharing my experiences with UDI requirements in the United States.

USDM Life Sciences, the leading risk management, technological innovation and business process optimization firm for the life sciences and healthcare industries announces Jay Crowley and Grant Hodgkins will lead three discussions about EU MDR/IVDR requirements at the MDR & IVDR EU Conference 2017 in Orlando, FL December 5-6, 2017.

The US and EU MDR/IVDR UDI Requirements – Similarities, Differences and Implementation Issues

  • When: Tuesday, December 5, 2017 at 11:30am
  • Where: Hilton Orlando in Orlando, Florida
  • USDM Speaker: Jay Crowley, Member of MedTech Europe UDI and Eudamed Committees, Vice President – UDI Services and Solutions, USDM Life Sciences

The New Enhanced Responsibilities of Other Economic Operators

  • When: Wednesday, December 6, 2017 at 10:15am
  • Where: Hilton Orlando in Orlando, Florida
  • USDM Speaker: Jay Crowley, Member of MedTech Europe UDI and Eudamed Committees, Vice President – UDI Services and Solutions, USDM Life Sciences

Key to Success: Systems and Programs to Manage Complex Master Data Management

  • When: Wednesday, December 6, 2017 at 11:30am
  • Where: Hilton Orlando in Orlando, Florida
  • USDM Speaker: Grant Hodgkins, Member of GS1 Healthcare Global Leadership Team & Data Excellence Board, the SMU Big Data Advisory Board, and Vice President of Supply Chain Solutions, USDM Life Sciences

“I am looking forward to facilitating some critical discussions surrounding the MDR and IVDR requirements and sharing my experiences with UDI requirements in the United States,” said Crowley. “This event comes at a critical time for the medical device industry as the first MDR/IVDR deadlines approach and more countries around the world move towards implementing UDI regulations.”

At USDM Life Sciences, Crowley helps medical device manufacturers achieve regulatory compliance as well as internal benefits and competitive advantage with UDI implementation and MDR/IVDR guidance. Crowley held various positions over nearly 27 years at the FDA. Most recently, he was Senior Advisor for…

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