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News and Insights

Blog

FDA Letter to Industry Calls on Device Sponsors to Independently Verify Third-Party Data … Read more

Event

Visit our team during AMDM’s 50th Annual IVD Regulatory Meeting & FDA IVD Submission Workshop from April 22-25, 2024.… Read more

Blog

At-Home, POC, DCTs & Hybrid Models: IVD Expertise Across Every Use Setting … Read more

Blog

Regulatory Insights to Meet Evolving IVD QMS Requirements: LDTs, IVDR, & QSR to ISO 13485:2016 … Read more

Why Beaufort?

Beaufort’s team of experts are at the core of our success. We support one another to grow and refine our expertise for the benefit of our partners. Because, when we come together for the success of our clients, we achieve results we all can be proud of.

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