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Heike Kenngott is an accomplished regulatory affairs professional with extensive experience in the pharmaceutical industry. Currently serving as Vice President of Regulatory Affairs at Gedeon Richter - PregLem S.A. since October 2016, Kenngott previously held significant roles at Merck Serono S.A., including Regulatory Affairs Director for Biosimilars and Director of Global Regulatory Affairs in Endocrinology. Kenngott's career in regulatory affairs began at Serono, progressing from an Associate Manager to an Associate Director, while also gaining experience as a Clinical Compliance Auditor. Earlier roles include serving as Regulatory Affairs Officer at Merck KGaA. Educational qualifications include a Master of Science in Pharmaceutical Medicine from the University of Surrey and a Dipl-Ing (FH) in Chemistry from Fachhochschule Isny.