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Entering the US medical device market: classification and premarket pathways

Before launching a medical device in the US, manufacturers must understand FDA classification and select the appropriate premarket pathway. This guide outlines key steps for successful market entry.

06/26/2025
Maria Manzano 2025-06-26T05:58:38+00:00
News

Washington State introduces interim policy on lead in cosmetics

Discover the effects of non-compliance with the Modernization of Cosmetics Regulations Act of the FDA to your business and market access.

01/22/2025
Maria Manzano 2025-01-22T16:22:52+00:00
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