Hey Product Hunt! I’m Gauri Kundliya, co-founder of Gamura. We built Gamura because navigating medical device regulations is overwhelming, especially for startups, MSMEs, and consultants who juggle multiple markets. What Gamura does today ✨ AI chatbot for QA/RA and compliance 🌍 Covers regulations in 18 countries 📜 From US FDA (21 CFR framework) to EU MDR to Indian MDR 2017 and beyond ⚡ Instant, conversational answers → less manual research, more audit-readiness Who it’s for - MedTech startups trying to get market entry right the first time - MSMEs needing cost-effective QA/RA support - Consultants who manage clients across multiple regions Our story: As a QA/RA professional myself, I’ve seen how much time (and stress!) goes into chasing down clauses, preparing for audits, and keeping up with evolving rules. We wanted a tool that felt like a compliance co-pilot, always there when you need quick, reliable guidance. Our goals with this launch: We’d love your feedback on usability and accuracy; how does Gamura fit into your workflow? What would make it indispensable for you? Thanks for checking out Gamura. Excited to hear your thoughts and learn from this community! 🙏

Gamura AI

Navigate Medical Device Regulations with AI

Navigate Medical Device Regulations with AI