Lori Pfohl Email & Phone Number

With over 30 years of experience in the medical device industry, I am a seasoned regulatory affairs professional with a track record of success in leading regulatory affairs, quality, and sterilization projects. I have authored and submitted more than 10 510(k) applications for various medical devices, and ensured compliance with FDA and international standards and regulations.As a Regulatory Affairs Team Lead at Teleflex, I managed a team of regulatory affairs specialists and coordinated regulatory strategies and activities for multiple product lines and markets. I also supported the quality and sterilization functions, conducting audits, tender submissions, and ISO certifications. My mission is to leverage my regulatory affairs expertise and leadership skills to facilitate the development and launch of innovative and safe medical devices that improve patient outcomes and healthcare quality.

Listed skills include Regulatory Affairs, Validation, Iso 13485, Fda, and 46 others.

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  State University Of New York College At Plattsburgh

  Chemistry, In Vitro Cell Biology And Biotechnology