FD-AID LLC was founded and is run by DeVaughn Edwards, a pharmaceutical quality and regulatory consultant with 14 years of experience as an FDA Investigator and 13 years in pharmaceutical quality leadership, including work on the team that navigated Johnson & Johnson out of a consent decree. The FD-AID team are a group of former FDA Investigators and pharma industry executives who have the experience to know the effective paths of compliance.

Every template, guide, and framework sold here reflects the same standard applied in live FDA inspections and consent decree remediation work, not textbook theory. If you're a quality or regulatory professional who needs tools built by someone who has sat across the table from an FDA Investigator and also been the one issuing the findings, you're in the right place.

Questions before you buy? Reach out directly: devaughn@fdaid.org