معرفی
Timothy G Philips serves as an Instructor in the School of Engineering at the University of St. Thomas, specializing in Regulatory Science and Medical Device Development. With over 30 years of experience at the U.S. Food and Drug Administration (FDA), he brings extensive expertise in medical device regulation, quality systems, and compliance to his academic role.
His educational background includes a Bachelor of Science in Biomedical Engineering from the University of Iowa. Mr. Philips' research and teaching focus centers on FDA regulatory frameworks for medical devices, covering pre-market submissions (510(k), PMA), quality management systems, inspection protocols, evidence development for enforcement actions, and post-market compliance with emphasis on product recalls and surveillance.
No scientific awards were documented in the provided information.
In his current teaching capacity, Mr. Philips instructs ETLS 721: Medical Device Regulatory Submissions, which explores regulatory pathways from investigational device exemptions to pre-market approvals and international harmonization standards. While no formal graduate students are listed, his coursework involves mentoring students in regulatory strategy development and compliance implementation.
No laboratory facilities or dedicated research teams under his direction were specified in the source material.
