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Christian Podolak has a strong background in regulatory affairs and validation within the medical technology industry. With experience in companies like corpuls | GS Elektromedizinische Geräte G.Stemple GmbH, Smiths Medical, Stryker, and Fraunhofer IIS, Christian has held various roles such as Vice President Quality Management & Regulatory Affairs, Global Project Manager MDR, and Regulatory Affairs Specialist. Christian graduated from Hochschule München University of Applied Sciences with a degree in Biomedizintechnik/Medizintechnik.