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Unpacking Averages: Assessing the Products Included in FDA's Voluntary Malfunction Summary Reporting Program | Epstein Becker & Green

Unpacking Averages: Assessing the Products Included in FDA's Voluntary Malfunction Summary Reporting Program | Epstein Becker & Green
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Reviewing FDA VSMR Manufacturer Draft Guidance

Reviewing FDA VSMR Manufacturer Draft Guidance
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2 Day Medical Device Post-Market Regulations and Challenges

Dublin, Dec. 30, 2022 (GLOBE NEWSWIRE) The "A Comprehensive View of Medical Device Post-Market Regulations and Challenges -Complaint Handling, MDR. ....

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Navigating the Medical Device Post-Market Maze and Challenges During COVID-19 Pandemic Online Seminar - Learn what FDA is Really Thinking on Regulation and Guidance Documents (May 13-14, 2021)

Navigating the Medical Device Post-Market Maze and Challenges During COVID-19 Pandemic Online Seminar - Learn what FDA is Really Thinking on Regulation and Guidance Documents (May 13-14, 2021)
March 10, 2021 05:33 ET
| Source:
Research and Markets
Research and Markets
Dublin, IRELAND
ResearchAndMarkets.com s offering.
Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time-consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas.
By attending this seminar, you will discover:
How to overcome one of the biggest obstacles device manufacturers face
How the FDA expects you to develop and implement proper handling of complaints reportable or non-reportable, product complaint handling, and documentation ....

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