SILVER SPRING, Md.—American Herbal Products Association’s (AHPA) revision to the AHPA Guidance on How to Conduct an FDA Inspection is now available. It was revised by AHPA president Michael McGuffin; AHPA general counsel/partner at Kleinfeld, Kaplan & Becker Tony Young; and government relations committee chair/VP of quality at Cortex Scientific Staci Eisner. t guidance will assist you before, during and after an inspector arrives at the door of your manufacturing facility and conducts an inspection.
The 51-page guidance gives a solid understanding of your rights and obligations, and the FDA's authority, during an inspection under the dietary supplement cGMP (current good manufacturing practice) and is broken down into four sections, presented in a question and answer format, and two appendices.
