US Food and Drug Administration
Ms. Angela Krueger serves as the Deputy Director for Regulatory Policy for the Office of Product Evaluation and Quality (OPEQ), Center for Devices and Radiological Health (CDRH) at the US Food and Drug Administration (FDA). In this position, she provides executive leadership regarding regulatory policy issues that impact the premarket and postmarket review of medical devices for OPEQ. Ms. Krueger provides oversight and strategic direction for OPEQ’s policy, guidance, and regulation development and implementation teams, including in areas such as digital health, combination products, and device-specific policy. Ms. Krueger has worked at the FDA for over 20 years and has previously served in the former Office of Device Evaluation (ODE) as the Deputy Director for Engineering and Science and Associate Director for Regulations and Guidance; a Regulatory Advisor and Policy Analyst; CDRH Product Jurisdiction Officer; and a Scientific Reviewer in the Division of Cardiovascular Devices. Ms. Krueger holds degrees in Chemistry and Journalism from Butler University, Indianapolis, Indiana.
Health Authority Forum: CDRH - FDA's Center for Devices and Radiological Health
Wednesday, September 18, 2024
2:15 PM – 3:15 PM PDT