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Monday, June 21 • 10:00am - 11:30am
Microneedling FDA Regulatory Updates

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In November 2020, the Food and Drug Administration released a guidance document that provides guidance on when micro-needling devices are considered to be medical devices. This session will discuss the implications of the guidance to persons providing micro-needling services. In addition, the presentation will outline things to ask from micro-needling suppliers, what marketing pit falls to avoid, and how to continue to be competitive.

Speakers
avatar for Maria Golovina

Maria Golovina

Regulatory Affairs Expert
Maria Golovina is a certified esthetician with 11 years of medical regulatory project/program management experience, as well as numerous acquisition projects. Her areas of expertise include program management, software (stand alone and embedded), orthopedics, IVD, ophthalmic, microsurgery... Read More →


Monday June 21, 2021 10:00am - 11:30am PDT
Room N113