Got Observations?: Ensuring Effective Responses to FDA 483s and Warning Letters

Recorded January 21, 2026 | 12:00PM–1:30PM ET | On-Demand Webinar

Overview

Join our panel of experts for a practical deep dive into effectively responding to FDA 483s and Warning Letters. This webinar, tailored especially for the life sciences industry, features real-world case studies and actionable strategies to help you avoid escalation and safeguard your organization’s credibility following notification of FDA inspection observations. Learn how to develop thorough, well-reasoned responses to these notices, identify common pitfalls, and align your approach with FDA’s expectations.

$149

Members

$249

Non-Members

Speakers

Donald Ashley
Read Bio
Principal, Regulatory Compliance, ELIQUENT Life Sciences

David Crome
Read Bio
Managing Director, Quality & Compliance UK, Ireland & India, ProPharma Group

Joe McGinnis
Read Bio
Senior Director, Pharmaceutical Regulatory Compliance—Americas, Johnson & Johnson

Moderated By Kalie Richardson
Read Bio
Director, Hyman, Phelps & McNamara, PC

FDLI applies for CLE credits in Ohio and Virginia. These CLE approvals also may be honored by other states. The CLE credits will be posted as they are granted and registrants can request to be notified when approval is received.