Rebecca E. Dombrowski, MS

Supervisory Investigator, ORA
U.S. FDA

Rebecca Dombrowski is a Supervisory Investigator in the Office of Regulatory Affairs, Division III. Previously, Rebecca was an Application Reviewer with CDER’s Office of Pharmaceutical Quality, under the Division of Inspectional Assessment, and subsequently, a Compliance Officer with CDER’s Office of Manufacturing Quality. With over 17 years of inspectional experience with the FDA, including 3 years as a District Pre-Approval Manager and 2 years as a Drug Specialist, Rebecca attained Level II and Level III certification as a drug investigator, and became a member of FDA’s Pharmaceutical Inspectorate. She holds a Bachelor of Science and a Master of Science in Biology, and has experience lecturing in both academic and agency forums.

Presentation(s):

• C3: Improving Manufacturing via Modern Technology

  Tuesday, September 28, 2021
  15:30 – 17:00 EDT

• Live Q&A (C3)

  Tuesday, September 28, 2021
  16:24 – 17:00 EDT

• Special Topic 5: AI Research Force (AIRForce) Group: Focus on Artificial Intelligence and Machine Learning

  Wednesday, September 29, 2021
  08:30 – 09:30 EDT

• Live Q&A (ST5)

  Wednesday, September 29, 2021
  08:55 – 09:30 EDT