Leo Heller

Leo Heller is a seasoned Regulatory & Development Consultant with extensive experience in quality management and regulatory affairs, particularly in the medical devices sector. They held positions such as Quality Assurance & Regulatory Affairs Manager at Dutch Ophthalmic Research Center and Director of QA & Supply Chain at Cassini BV. Leo has contributed to various organizations, including serving as a Sr. Project Associate at Xendo PharmaServices and leading MDR projects at BioClin. Currently, Leo is engaged as a Regulatory & Development Consultant at MD squared B.V., building on a solid foundation of education with an MSc in Business Administration from Erasmus University Rotterdam and a degree in Precision Engineering from Hogeschool Utrecht.