FALLS CHURCH, Va., May 16, 2019 /PRNewswire-PRWeb/ -- Part 806 Reports: When to Submit?
Is It a Device Recall … or Product Enhancement?
**An FDAnews Webinar**
Thursday, May 30, 2019, 11:00 a.m.-12:30p.m. EDT
https://www.fdanews.com/part806reports

Has your company undergone an FDA device recall? There is a difference between a recall and an enhancement?

What once was a product enhancement now may be considered a recall and, sometimes, neither enhancement nor recall. This is the moment to figure it all out. It's easily avoidable.

Join Covington & Burlington's Pamela Forrest Esq. in a chalk-talk on 21 C.F.R. 806, the regulation that spells out terms of device recalls. In 90 fast-paced minutes, attendees will discover the difference between a recall and a product enhancement and much more, such as:

•     21 C.F.R. Part 806: Nuances of the regulation, when to report a recall
•     Recall-specific terms: How recalls differ from enhancements
•     Part 806 pitfalls: Handling different classes of device recalls
•     Bad things that can happen: Enforcement actions, liability and more
•     Product seizures: They're among the worst of bad things

Product seizures are the worst but warning letters and Forms 483 aren't good news either. Don't expose the organization to sanctions and liability when the ins and outs of Part 806 can be easily mastered.

Click here to register and for more information.

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Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally
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Webinar Details:
Part 806 Reports: When to Submit?
Is It a Device Recall … or Product Enhancement?
**An FDAnews Webinar**
Thursday, May 30, 2019, 11:00 a.m.-12:30p.m. EDT
https://www.fdanews.com/part806reports?hittrk=19516VOCUS

Tuition:
$287 per site

Easy Ways to Register:
Online: https://www.fdanews.com/part806reports?
By phone: 888-838-5578 or 703-538-7600

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FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

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