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A service for medical industry researchers · Tuesday, May 13, 2025 · 812,333,748 Articles · 3+ Million Readers

Former FDA Investigator Launches Global FDA Inspection Masterclass Video for Pharma and Biotech Compliance Teams

FDA Inspection Masterclass promotional image featuring gold text on a dark background, highlighting “Former FDA Investigators’ Guidance” and presented by DeVaughn Edwards, CEO of FD-AID, LLC.

FDA Inspection Master Class

Global video course teaches inspection readiness strategies from former FDA Investigators—now available on-demand.

“We created this masterclass because far too many companies wait until an FDA inspection is scheduled to prepare. That’s usually too late.”
— DeVaughn Edwards, Principal Consultant, FD-AID, LLC
LUTZ, FL, UNITED STATES, May 13, 2025 /EINPresswire.com/ -- With FDA inspections becoming increasingly rigorous and the announcement from the FDA that international international companies will no longer be given a heads-up of a pending inspection, a new video masterclass created by former FDA Investigators is now available to help pharmaceutical and biotech companies worldwide better prepare for regulatory scrutiny.

FDA Inspection Masterclass: Former FDA Investigator’s Guidance” is a comprehensive, on-demand training course developed by DeVaughn Edwards, Principal Consultant at FD-AID, LLC. Edwards, a former FDA Investigator with 14 years of field experience and over a decade in the pharmaceutical industry, collaborated with other regulatory experts to create an insider-driven guide to surviving — and succeeding — in FDA inspections.

“This is the type of training I wish more companies had before we walked through the door,” said Edwards. “It covers what Investigators actually evaluate and how to avoid the most common and costly mistakes.”

The training includes eight modules covering:

- FDA inspection triggers

- PAI (Pre-Approval Inspection) strategy

- How to conduct internal mock inspections

- Interview techniques

- Real-world examples of Form 483 missteps

- Clinical and GMP-specific risks

Participants will receive:

- On-demand access to the full course

- Certificate of completion (optional)

An option for team-based licensing

With U.S. and global regulators increasing their oversight, especially of contract manufacturers and clinical operations, this video offers a critical opportunity to close compliance gaps before the FDA identifies them.

The course is now available internationally at:
https://devaughnedwards.podia.com/fda-inspection-masterclass-former-fda-investigator-s-guidance

About FD-AID, LLC
FD-AID, LLC is a pharmaceutical consulting firm led by former FDA Investigators and industry executives. The company provides mock FDA inspections, regulatory remediation, and GMP compliance training to clients around the world. More at www.fdaid.org.

Media Contact:
DeVaughn Edwards
Principal Consultant
FD-AID, LLC
devaughn@fdaid.org | +1 (732) 895-7831
5514 Garden Arbor Drive, Lutz, FL 33558

DeVaughn Edwards
FD-AID LLC
+ 17328957831
email us here
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