Jay Crowley to Present Challenges with EU MDR and IVDR Compliance
SANTA BARBARA, Calif., Aug. 1, 2019 /PRNewswire-PRWeb/ -- USDM Life Sciences (USDM) announces that Jay Crowley, Vice President of Unique Device Identification Services and Solutions , will deliver a detailed webinar addressing challenges with the upcoming EU MDR IVDR regulations .
- SANTA BARBARA, Calif., Aug. 1, 2019 /PRNewswire-PRWeb/ -- USDM Life Sciences (USDM) announces that Jay Crowley, Vice President of Unique Device Identification Services and Solutions , will deliver a detailed webinar addressing challenges with the upcoming EU MDR IVDR regulations .
- Prior to USDM, Jay was a Senior Advisor for Patient Safety in the Food and Drug Administration's Center for Devices and Radiological Health.
- He currently focuses on providing business process, technology and compliance solutions for the regulated life sciences industry at USDM.
- The presentation will include the following insights:
"EUDAMED database compliance requirements under the EU MDR and IVDR are only one year away, and medical device companies need a well-defined strategy to create a sustainable compliance plan," said Crowley.