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