Adam Kleinman
Associate Director, Medical & Scientific Writing | Medical Device Regulation Expert
- Role
- Associate Director, Medical & Scientific Writing at Philips
- Location
- Pittsburgh, PA, US
- LinkedIn followers
- 500 followers
About Adam Kleinman
At Philips, our focus is unwavering on elevating clinical compliance for hospital patient monitoring systems within stringent EU regulatory frameworks. In my role as Associate Director, Medical & Scientific Writing, I steward our team to ensure our HPM portfolio meets the exacting standards of EU regulations, leveraging my expertise in EU MDR and MEDDEV. Through process and workflow improvements, our team is now also publishing scientific articles and position papers with collaborators in healthcare and academia.Transitioning from a Medical Writer to Associate Director I have honed a distinctive skill set in drafting and maintaining clinical evaluation reports, a testament to Philips commitment to healthcare technology safety and performance. Our collaborative efforts are crucial in navigating the complexities of medical device regulation and upholding the integrity of clinical evidence.
Experience
Associate Director, Medical & Scientific Writing
Apr 2025 — Present
Lead the medical & scientific writing team for the Philips Hospital Patient Monitoring business unit. Ensure compliance to EU regulations (EU MDR, EU MDD) for HPM portfolio with the focus on clinical evaluation reports and post-market clinical follow-up reports, as well as writing scientific articles and position papers with healthcare and academic collaborators
Education
North Central College
Bachelor’s Degree, Biochemistry
2011 — 2015
University of Pittsburgh School of Medicine
Doctor of Philosophy - PhD, Microbiology and Immunology
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