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.
Interested in registering multiple sites?
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally
to learn about our special multisite discount.
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
About FDAnews:
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.
SOURCE FDANEWS