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Manufacturers and importers only have until August 13, 2015 to begin submitting all MDR reports electronically. Learn what you need to do to test and start submitting data by the FDA deadline. USDM Life Sciences and 123Compliance will also outline the different methods of submitting data and help you decide which option is best for your organization. We’ll also explain how moving your submission process to the Cloud provides a more efficient, effective, and time saving process.

  • Overview of the eMDR requirements
  • What you need to do now to start submitting data
  • eMDR submission options
  • Drag-and-drop regulatory reports in minutes
  • How to automate the submission process
  • Live Q & A session

About the Presenters:

David Blewitt

Vice President of Cloud Compliance David is an accomplished Life Sciences regulatory and IS compliance professional with extensive hands-on and leadership experience in the pharmaceutical, medical device, biotech and blood management industries. He is an acknowledged expert on a wide range of regulatory predicate rules.

Plarent Ymeri

CEO, 123Compliance With more than 14 years of experience in the life science and healthcare industries, Plarent brings direct knowledge and expertise of software organization leadership, development, implementation and validation.

Bryan Coddington

Bryan is an IT professional with in-depth knowledge of cloud, process optimization, integration, and mobile applications for the Life Sciences industry. A Digital Transformation (Dx) thought leader helping companies maximize their investment in cloud-based applications while remaining compliant with GDPR and federal regulations such as 21CFR Part 11, 803, and 820.

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