# Questions and Answers about eMDR - Electronic Medical Device Reporting - Guidance for Industry, User Facilities and FDA Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/questions-and-answers-about-emdr-electronic-medical-device-reporting-guidance-for-industry-user-facilities-and-fda-staff/ec55d45c-ba23-407d-959e-776337e921a3

> FDA guidance document: Questions and Answers about eMDR - Electronic Medical Device Reporting - Guidance for Industry, User Facilities and FDA Staff. Issue date: February 13, 2014. Get complete insights and analysis.

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## Details

- Title: Questions and Answers about eMDR - Electronic Medical Device Reporting - Guidance for Industry, User Facilities and FDA Staff
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 2014-02-13
- Last Changed: 2020-03-02
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2008-N-0393">FDA-2008-N-0393</a>

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