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Libet Garber, Ph.D. has been working in the medical device industry since 2006. Libet began their career as an Electrical Engineer at The Johns Hopkins University Applied Physics Laboratory. In 2009, they joined the FDA as a Biomedical Engineer/Scientific Reviewer, where they were responsible for leading reviews of complex cardiac medical devices to make safety and effectiveness determinations, as well as leading multidisciplinary teams throughout the total product life cycle of medical devices regulatory reviews. In 2019, they moved to Bovie/Apyx Medical as Global Director of Regulatory Affairs. Most recently, in 2020, they joined AtaCor Medical, Inc. as Director of Regulatory Affairs.

Libet Garber, Ph.D. obtained a Bachelor of Science and Engineering-BS from the Johns Hopkins Whiting School of Engineering in 2005, majoring in Biomedical/Medical Engineering. Libet then went on to pursue a Master of Science and Engineering- MSE from The Johns Hopkins University School of Medicine, which they completed in 2006. In 2012, they obtained their Doctor of Philosophy - PhD from the University of Maryland School of Medicine, majoring in Bioengineering and Biomedical Engineering. In 2019, they obtained a RAPS Member certification from the Regulatory Affairs Certification Program.