Regulatory, Quality & Compliance Consultant
Lisa Pritchard, BSEEE, is a Regulatory, Quality & Compliance Consultant at DuVal & Associates, P.A., a law firm dedicated to counseling companies in the medical device, pharmaceutical, biotech, food, and nutritional supplement industries. She focuses on advising clients on Regulatory, Quality and Compliance topics.
Lisa works extensively with assisting clients with worldwide regulatory strategies, marketing submissions and applications (FDA submissions including pre-submissions, 510(k)s, de novos, PMAs, advisory panel meeting preparation, etc.; European Design Dossiers and Technical Files, Canadian license applications, Australian listing applications, etc.); quality system strategies and compliance topics. Lisa brings over 25 years of experience in working with industry.
Prior to joining DuVal & Associates, she executed successful Regulatory, Quality and Compliance strategies at a variety of device companies including American Medical Systems, Medtronic, UroMedica, and EnteroMedics. She brings extensive experience in strategy development, submission preparation, regulatory body negotiations, advertising/promotional materials assessment, inspection/audit preparation and conduct, quality system design, risk assessment, development of design control documentation, usability evaluations, clinical trial design, and adverse event reporting. Lisa earned her Bachelor of Science, Electrical and Electronics Engineering, from North Dakota State University.
Lisa's Latest Events
- April 6, 2019 April Training Workshop: Making sense of FDA Land in Submissions (510(k)s, De novos, and PMAs)
- April 17, 2019 MedTech Monitor 2019: Industry Trends