Adam K. is an Associate Director of Clinical Compliance at Philips, where they focus on enhancing compliance for hospital patient monitoring systems within EU regulatory frameworks. They transitioned from a Medical Writer to this leadership role, leveraging their expertise in EU MDR and MEDDEV to ensure adherence to clinical evidence standards. With a PhD in Microbiology and Immunology from the University of Pittsburgh and experience as a consultant at RQM+, Adam has developed a unique skill set in drafting clinical evaluation reports and navigating medical device regulations. Prior research positions included virology work at Virginia Tech and conducting experiments at North Central College.
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