Principal, Consulting Services
RQM+
Torrie DeGennaro has a BS in Biomedical Engineering with a concentration in biomechanics, with over five years of professional medical device experience and has her Six Sigma Green Belt along with being a Certified Medical Device Auditor. Torrie has extensive post-market surveillance experience, authoring and reviewing hundreds of documents for regulatory submissions, including PMCF deliverables and PSURs. Torrie serves as key contributor to RQM+’s success in the collection of PMCF data for a variety of medical devices. Additionally, she has experience as a quality engineer for new product development and can provide the quality and regulatory perspective in new product development projects for initial market submissions. Torrie has extensive experience working with legacy devices to develop PMCF strategies for initial MDR submissions.
Disclosure information not submitted.
Sponsored Presentation: Unlocking the Power of Retrospective PMCF Studies for EU MDR Compliance
Thursday, October 5, 2023
12:15 PM – 12:40 PM EDT