Freyr provides India CDSCO medical device registration and approval support for device manufacturers that includes registration, classificat
🩺 Looking to register your Medical Devices in India? Let Freyr be your regulatory partner for CDSCO compliance and fast-track market entry!
📌 At Freyr Solutions, we offer end-to-end Medical Device Regulatory Services in India – covering everything from classification to CDSCO submissions and licensing.
🔍 Our Expertise Includes: ✅ Device classification (A, B, C, D) under MDR 2017 ✅ Import & manufacturing license support (Forms MD-14/15, MD-3/6) ✅ Indian Authorized Agent services ✅ QMS Documentation (ISO 13485) ✅ UDI, labeling & post-market vigilance ✅ CDSCO interactions and regulatory strategy
💡 Whether you’re a foreign manufacturer or an Indian distributor, we ensure your devices are compliant, registered, and ready for launch — with zero regulatory stress.
📞 Get compliant. Get to market. Get Freyr. 🔗 Learn more: https://www.freyrsolutions.in/medical-devices-regulatory-support-in-india
