Live Webinar Understanding and Applying the New EU Medical Device Regulations (EMDR)

By: David R. Dills ,Global Regulatory Affairs & Compliance Consultant and President, NovaQual.

The New EU MDR — Are You Really Ready? Your Roadmap to World-Class Implementation of Europe’s New Medical Device Regulation. You have 3 years to

  • 08-May-2018| 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute

Live Webinar Construct and Manage the Technical File and Design Dossier

By: David R. Dills ,Global Regulatory Affairs & Compliance Consultant and President, NovaQual.

A brief summary of manufacturing processes (flow chart including inspection and preventive monitoring steps) and validation of sterilization processes should be included in the design

  • 12-June-2018| 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute

Live Webinar FDA’s Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List

By: David R. Dills ,Global Regulatory Affairs & Compliance Consultant and President, NovaQual.

This Webinar will provide latest update as well as a “refresh” overview on how to register your device company and list your device(s) correctly and

  • 22-May-2018| 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute
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