You're invited to join the Atlanta Chapter for its annual virtual Breakfast with the Atlanta Southeast District FDA Office, Friday, December 2 (9:00 a.m.– 11:00 a.m. ET). 2 RAC Credits.
Don't miss out on this special opportunity to hear FDA representatives from the Atlanta District/Southeast Region discuss the latest compliance and enforcement-related topics.
During the interactive, two-hour webcast, attendees can ask questions and learn what issues their colleagues are tackling.
Anne E. Johnson is the Program Division Director of the Office of Bioresearch Monitoring Operations, Division 1, within the Office of Regulatory Affairs in the FDA. She directs field inspectional operations covering FDA-regulated clinical and non-clinical research, post-marketing pharmacovigilance, and select pre-approval programs designed to ensure human subject protection, evaluate data quality and integrity in product approval applications, and assess industry conformance with laws and regulations.
Ingrid Zambrana HAFE3 PDD began her career with Food and Drug Administration as a Consumer Safety Officer in 2000. She's served as the District Director of the FDA Atlanta District Office since April 2014. In 2016, Zambrana's leadership responsibilities expanded to include the title of Program Division Director charged with aligning operationally within the Office of Human and Animal Foods Operations.
Mark W. Rivero is a Compliance Officer in the Office of Pharmaceutical Quality Operations, Division 2, within the FDA Office of Regulatory Affairs. He specializes in the enforcement and regulatory follow-up in pharmaceutical manufacturing and compounding drug industries worldwide. His division covers the southeastern third of the United States including Puerto Rico and the U.S. Virgin Islands.
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