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FAQ

Common questions

Is GORA AI regulatory advice?

No. GORA AI provides informational guidance for planning and product development. Real submissions require qualified regulatory review and company-specific evidence.

Which markets do you cover?

EU MDR, FDA/CDRH, Swissmedic, China NMPA, Japan PMDA/MHLW, Brazil ANVISA, and Australia TGA — with more on the roadmap.

Can I try it before talking to sales?

Yes. Create a workspace and run a device through the full classification and dossier workflow right away.

How is your AI kept trustworthy?

The assistant answers only from curated source records and cites them. When source coverage is insufficient, it tells you instead of guessing.