FDA Regulatory Expert Shares Deep Dive on Draft Guidance for Conducting Hazard Analysis

In the following video interview, QA Magazine sits down with Ariel Seeley, of counsel at Morgan Lewis, to discuss FDA's draft guidance for conducting hazard analysis under FSMA, how the final guidance will affect food and beverage manufacturers, what FDA is currently prioritizing in its Human Foods Program and more.

Seeley draws on her knowledge of the FDA to provide strategic counsel on all aspects of regulation, compliance and enforcement. With FDA experience spanning multiple administrations and roles, she leverages her familiarity with FDA’s laws and regulations to advise clients on regulatory and enforcement matters, including helping clients with efficient and effective premarket strategies and to develop and implement effective compliance approaches.