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2022 State of the Medical Device Industry: Quality, Biocompatibility, and Changing Regulations

Published Date: March 15, 2022

Another year is here with regulatory changes, updated mandates, and the continued effects of the COVID-19 pandemic. Join leaders from Nelson Labs and Greenlight Guru to discuss the current state of the industry and forecast for 2022.

For each of the three areas listed below, this webinar discusses what the impending changes are, when these changes may take affect, and how medical-device manufacturers should prepare today.

  • Increasing importance of quality
  • Changes to ISO 10993-1
  • The end of the EUA


Learn more about the presenters below.

Thor Rollins

Thor Rollins

Biocompatibility Expert

Thor Rollins is a certified microbiologist and specializes in the selection and conduct of in vitro and in vivo biocompatibility tests. He actively speaks on biocompatibility related topics through Nelson Labs’ external seminars, webinars, and tradeshows. He presented on biocompatibility at the American College of Toxicology annual meeting in 2013 and has published many articles...


Etienne Nichols

Etienne Nichols is a medical-device guru and mechanical engineer who loves learning and teaching how systems work together. He has experience in manufacturing and also product development. He has aided in the development of combination drug-delivery devices, from startup to Fortune 500 companies. He holds a Project Management Professional (PMP) certification. Having managed cross-functional teams to update designs of legacy products, Etienne understands the pain of following the design-controls process in paper-based QMS environment. His expansive knowledge, experience, and passion with medical devices is evenly matched with how much he enjoys helping customers work efficiently through the design and development process to bring safe, high-quality products to market.

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