Are you a medical device manufacturer or importer preparing to comply with the FDA’s electronic adverse event reporting mandate? The countdown to the August 2015 deadline has already begun, but fear not. Pilgrim is here to help you get ready.

We’ve done the research and have shared our insider tips and resources to help you build your plan for eMDR compliance.

Download this presentation to learn:

  • What has been mandated?
  • What needs to be done before the deadline?
  • What is the process to register with the FDA?
  • How long will it take?
  • What options exist for electronic MDR submission?

Download this webinar to learn more. »

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