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Katrin Eva Canbulat serves as the Regulatory and Strategic Development Manager at Clinipace Worldwide since November 2016, specializing in quality and regulatory consulting and regulatory project management. Prior to this role, Katrin held several positions at GlaxoSmithKline Pharma GmbH from January 2012 to September 2016, including LOC Quality Lead and QP deputy, responsible for establishing audit plans and leading quality harmonization projects. Earlier experience includes serving as a Quality & Regulatory Officer at GlaxoSmithKline Consumer Healthcare AG from May 2009 to December 2011, where responsibilities included complaint handling and lifecycle management of consumer products, and as a Regulatory Affairs Manager at Schwarz Pharma from April 2007 to April 2009, focusing on compiling regulatory documents for markets in the EU and US. Katrin obtained a Diplom-Ingenieurin (Dipl.Ing.) in Pharmazie from OWL University of Applied Sciences and Arts in 2007.