Sandra A. Boyd

Drug National Expert
U.S. FDA

Sandra A Boyd is a Program Expert, Drug Specialist in the Pharmaceutical Quality Program Branch. Sandy has been with the FDA for 12 years with a focus in the area of drug manufacturing, current good manufacturing practice (CGMP) inspections, and related policy. Prior to becoming a Program Expert, Sandy spent her time performing complex drug inspections, including 4 years on the Dedicated Foreign Cadre, training other CSOs, and lecturing in both academic and agency forums. Prior to joining FDA, Sandy was the Director of Quality Systems and a Certified Quality Auditor for an API manufacturer and has worked in the pharmaceutical industry for 18 years. She recieved her BS degree from the University of Eau Claire.

Presentation(s):

• Inspection-Based Panel Discussion

  Monday, September 27, 2021
  15:30 – 16:17 EDT

• Inspection-Based Live Q&A

  Monday, September 27, 2021
  16:17 – 17:00 EDT

• Live Q&A (A2)

  Tuesday, September 28, 2021
  14:30 – 15:00 EDT