#pharmaceuticalregistration

Entering the UAE pharmaceutical market requires navigating a highly regulated environment. Herms Global provides expert solutions for Pharmaceutical/medicinal product registration in UAE, helping healthcare and pharmaceutical companies comply with MOHAP and other regulatory authorities.

From dossier preparation and classification to submission and follow-up, our regulatory affairs team ensures every requirement is met to streamline your market access. We support registrations for generic drugs, branded pharmaceuticals, herbal medicines, and more.

💡 Why choose Herms Global?

Extensive knowledge of UAE and GCC pharma laws

Fast, accurate documentation

Reduced risk of compliance failure

Dedicated regulatory consultants

🚀 Planning to register your pharmaceutical product in India? 📋 Don't let regulatory hurdles slow you down!

At Freyr Solutions, we simplify the entire Pharmaceutical Product Registration process as per CDSCO & DCGI guidelines – from dossier compilation to post-approval compliance.

✅ CTD/eCTD dossier preparation ✅ DCGI submission strategy ✅ Site registration & import license (Form 41, Form 10) ✅ Local representation & regulatory consulting ✅ 100% compliance with India’s regulatory framework

💡 Whether you're a domestic pharma company or an international manufacturer looking to enter the Indian market, Freyr ensures speed, accuracy, and regulatory clarity every step of the way.