#freyrsolutions

🩺 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.

🍱 Looking to Launch a Food Product in India? We've Got You Covered! 🇮🇳

Bringing a food or dietary supplement to the Indian market requires more than just a great product — it needs the right FSSAI approvals, documentation, and expert guidance to navigate the regulatory maze.

At Freyr Solutions, we specialize in end-to-end Food Product Registration services in India, helping you achieve fast and seamless compliance with FSSAI regulations.

🔍 Our Services Include: ✅ FSSAI License & Product Approval ✅ Ingredient Review & Label Compliance ✅ Import Clearance Support ✅ Post-market Surveillance & Renewals

💼 Whether you’re a domestic startup or an international brand, Freyr ensures your products hit the shelves without regulatory delays.

🚀 Launch with confidence. Stay compliant. Trust Freyr.