FOR FDA CONSULTANTS

Let AI handle the docs. Get back to consulting.

SittuAI drafts the documents required for 510(k), De Novo, and PMA submissions so you can focus on expert validation. Join for free and get matched with medical device and SaMD companies actively looking for regulatory expertise.

Free to Join. No Joining Fees.
Qualified client leads. We route medical device companies to consultants on our platform.
50% faster submissions. Validated by a working FDA consultant on a live engagement.
Your expertise, amplified. You validate every document — AI just handles the drafting grind.
Enterprise-grade privacy. SOC 2 compliant, HIPAA-ready, Azure-deployed.

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