Lisa Casavant is Cofounder and Executive Vice President of Regulatory and Quality Solutions (R&Q), an industry-leading regulatory and quality consulting firm that helps medical device and combination product companies bring safe and effective products to market… and keep them there. Lisa has been championing R&Q’s mission of improving lives since 2008, and has helped grow R&Q’s team to more than 100 industry experts who thrive in an entrepreneurial, collaborative, and fun-loving culture. Having a thorough understanding of the ever-changing global regulations is only half of it. Lisa is truly set apart by her success implementing regulations at multinational medical device companies, delivering business-balanced solutions for their business-balanced demands. R&Q’s clients look to Lisa and her team for forward-thinking insight and industry-best implementation of regulatory affairs. Lisa holds a Masters degree in Mechanical Engineering from the University of Delaware, along with a Bachelor of Science degree in the same subject from West Virginia University.
Conference Track: Post market surveillance under EU MDR – do I have to run a clinical study? What other options do you have to fulfill post market surveillance requirements; including updating CERs
Conference Track: Achieving MEDDEV 2.7/1 Rev. 4 and EU MDR Compliant Clinical Evaluation Reports (CERs): What We’ve Learned From Completing 100+