Global Regulatory Lead – Medical Device Regulatory Compliance Unit, Gedeon Richter Plc.
David Rathert has accumulated 28 years of experience with medical devices and combination products in the fields of Research & Development, Regulatory Affairs, Manufacturing, and Commercialization, and Quality Assurance and Quality Control. He is an experienced leader of multinational and multidisciplinary product design and development teams and has managed many complex international projects; often involving extensive interaction with customers and collaborative partners both internally and externally. David joined Gedeon Richter’s Medical Device Regulatory Compliance Unit in his current role as Global Regulatory Lead in July of last year. Prior to this he spent almost ten years consulting within the pharmaceutical industry; assisting companies such as Novartis, Roche, and Fresenius Kabi with their combination product development, market authorizations, and technology transfers.
