Daniela Zaczek is a Regulatory Affairs Director at Philips, where they plan and execute global regulatory submission activities and support new product development. Previously, they managed regulatory affairs at Rakuten Medical and DJO Global, overseeing clinical trial applications and global submissions for orthopedic products. Daniela holds a Bachelor's degree in Biomedical Engineering and Chemistry from the University of Pittsburgh and has completed internships focused on research and quality control in various engineering contexts. They are certified as a CQE and RAC-US.
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