FDA Device eSubmission Pilot

The FDA is accepting requests to participate in its Medical Device eSubmission pilot program. This is only open for devices being submitted to ODE’s Division of Cardiovascular Devices Cardiac Diagnostic Devices Branch or Peripheral
Interventional Devices Branch. This will be interactive to evaluate the process/tools and the Refuse to Accept screening will be waived for participants. Deadline for requests to participate is September 30, 2014.

What’s New

FDA:  Exemptions, Variances, and Alternate Forms of Adverse Event Reporting for Medical Devices

Manufacturers, importers, and user facilities can request an exemption or variance from any or all of the medical device reporting requirements in 21 CFR Part 803.  Read more:  https://www.fda.gov/medical-devices/medical-device-reporting-mdr-how-report-medical-device-problems/exemptions-variances-and-alternate-forms-adverse-event-reporting-medical-devices

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