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Beate R. Schmidt, MSc, MDRA, RAC

Consultant
Benefits Regulatory Consulting

Beate R. Schmidt is a freelance regulatory consultant with more than 20 years of experience in drug development and licensing. A biologist by training, she also holds a Master's degree in Regulatory Affairs (MDRA) as well as RAC credentials for the US and EU. Beate has worked in the pharmaceutical and biotech industry in Europe, US and Canada, where she helped advance various global drug development programs. From 2009-2012 she was a Product Team Leader (PTL) at the European Medicines Agency (EMA) in London. More recently, she has expanded her academic training and professional work on areas of market access, drug pricing & reimbursement as well as drug-device combination products. She holds a Master's degree in Health Economics, Policy & Management (HEPM) from the London School of Economics (LSE) and obtained a Market Access Manager Certificate from the European Business School (EBS). From 2013-2017 Beate functioned as the European Liaison for RAPS.

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