Background - Practices (Details)

Mass Tort, Product, and Consumer Litigation


FDAnews Webinar - FDA 483s & Warning Letters What Regulatory and Quality Professionals Absolutely Need to Know

November 25, 2019 • Webinar

Starts: 1:30 PM (EST)
Ends: 3:00 PM (EST)

Doing an annual lookback at the 483s and warning letters the FDA has issued can provide great insights to prepare you for your next inspection and will give you a glimpse of some of the areas the FDA is focusing on. There are top citations that come up year after year, such as insufficient CAPA investigations and not following your SOPs, but new patterns crop up all the time. Join us for a new analysis of the trends and what you can do to pass your next inspection with flying colors.

Partner John Fuson and counsel Chalana Damron will be presenting this webinar titled "FDA 483 and Warning Letter Trends" on Monday, November 25th at 1:30 pm.
Crowell & Moring Participant(s):
John Fuson
Partner – Washington, D.C.
Phone: +1 202.624.2910
Chalana N. Damron
Counsel – Washington, D.C.
Phone: +1 202.624.2566
For more information, please visit these areas: