Marc Palgen is a Regulatory Affairs and Quality Manager specializing in medical devices and in vitro diagnostics. With an engineer's degree in biomedical engineering, they have amassed extensive experience in regulatory affairs, working at organizations such as Philips, Stago, and Cerba Xpert. Currently, they are focused on regulatory affairs at Philips, drawing on their expertise in various regulations and quality standards, including MDR and IVDR. Marc's interest in international collaboration, particularly in relation to Chinese culture, complements their professional endeavors.
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