Dennis C. Gucciardo

Appealing A Denial Of A Drug/Medical Device Export Certificate: FDA Final Guidance

FDA Delays Draft Rule For QSR/ISO 13485 Harmonization

Your QMS Supports Your Global Operations And We Are Prepared To Support You

FDA Addresses Industry Feedback On Routine Inspections By Formalizing Processes And Standards In A Draft Guidance

FDA Issues Final Guidance For Public Warnings And Notification Of Recalls