Doug Kentz
Director of Regulatory Affairs at Philips
- Role
- Director of Regulatory Affairs at Philips
- Location
- Milwaukee, WI, US
- LinkedIn followers
- 500 followers
About Doug Kentz
Collaborative, strategic and solutions-oriented Regulatory Affairs Leader with significant medical device regulatory affairs managerial and technical experience. Thorough understanding of bringing medical devices to market with cross-functional product development teams under QSR/GMP regulations and ISO 13485 QMS requirements using sound global regulatory strategies. Led and developed global regulatory teams of up to twenty-one RA Managers and Leaders. Extensive US (510(k), IDE and PMA), EU and international registration experience. Medical device experience includes CT, patient monitoring, ECG analysis, automated drug delivery, surgical, implantable, and IVD devices
Experience
Director of Regulatory Affairs
Sep 2018 — Present · Milwaukee, WI, US
Responsible for global regulatory affairs supporting the Computed Tomography and Advanced Molecular Imaging Business (CT, Spectral CT, and PET/CT Systems including image reconstruction algorithms and AI-based image reconstruction algorithms). Lead, manage and develop Regulatory Managers and Leaders at multiple sites around the world.
Education
University of Illinois at Urbana-Champaign
BS
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