Anne P.

Anne P. is an experienced regulatory affairs professional with a strong background in medical device compliance, currently serving as Associate Manager of Regulatory Affairs at Medline Industries, LP since November 2017. Expertise includes managing regulatory activities for the EU and Australia markets, focusing on EU MDR 2017/745 compliance, UKCA regulations, and risk management as a Subject Matter Expert in EN ISO 14971. Previous roles encompass positions at Baxter International Inc. as Quality Engineer I, where Anne led quality efforts for nutrition product families, and at Zimmer Biomet as a Trauma Product Development Co-op. Educational credentials include a Bachelor’s Degree in Bioengineering and Biomedical Engineering from Miami University.