Review-Based Panel Discussion

Moderator(s)

• 

  Denise M. DiGiulio

  Head of Global Audit and Inspection Management
  Genentech
  West Chester, Pennsylvania, United States
• 

  Mary E. Farbman, PhD

  Associate Vice President, Global Auditing and Compliance Support
  Merck & Co., Inc.
  Newton, Massachusetts, United States

Regulatory Panelist(s)

• 

  Kristen L. Anderson, PhD

  Microbiologist, CVM
  U.S. FDA
  Derwood, Maryland, United States
• 

  Bing Cai, PhD

  Division Director, CDER
  U.S. FDA
  Potomac, Maryland, United States
• 

  Patricia F. Hughes, PhD

  Senior Scientific Advisor, CDER
  U.S. FDA
  Silver spring, Maryland, United States
• 

  Derek S. Smith, PhD

  Deputy Director, Office of Pharmaceutical Manufacturing Assessment, OPQ, CDER
  U.S. FDA
  Columbia, Maryland, United States