dicentra

FDA

dicentra is a Toronto-based regulatory consulting firm and CRO serving medical device and other health-product companies. Its device team provides FDA and Health Canada regulatory strategy, agency liaison, submission support, clinical trial planning and post-market reporting. For diagnostics, wearables and software-driven devices, dicentra also supports 510(k), De Novo, PMA and Q-Submission evidence planning and regulator engagement.

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