Navigating PFAS in Medical Devices
About the Webinar
In recent years, the medical device industry has found itself at the crossroads of innovation and regulation, particularly with the increasing scrutiny over the use of per- and polyfluoroalkyl substances (PFAS). Known for their chemical resistance, heat resistance, durability, lubricity, and biocompatibility, PFAS have been integral in manufacturing medical devices. Their persistence in the environment and potential health risks have led to sweeping global regulatory actions that are starting to impact the medical device industry.
In this webinar, our experts examine the impact of recent and anticipated regulations on medical devices, and share what we’ve learned for strategic insights, solutions, resources and more for adapting to this evolving landscape.
What You'll Learn
PFAS Overview
Regulations and Impact
Strategies and Solutions
FAQs and Resources
Featured Experts
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Shalene Thomas, R.E.P
Sr. Emerging Contaminants Program ManagerShalene provides thought leadership, drives R&D and service offerings for Battelle’s growing PFAS and other potential emerging contaminant programs. She has more than 25 years of experience in environmental consulting that includes 15 years of experience providing PFAS strategic management services to government and commercial clients. -
André LaFreniere
Vice President, Medical Device SolutionsAndré LaFreniere leverages his 20 years of experience in healthcare technology to advance opportunities and solve challenges in healthcare. Andre’s product development and commercialization knowledge spans collaborations with commercial clients across pharmaceuticals, biotechnology, medical devices, diagnostics, and healthcare systems to solve complex problems and change healthcare for the better.