At Global MedRegs, we recognize the challenges medical device manufacturers face in navigating diverse and ever-evolving international regulations. Our mission is to simplify the complex regulatory landscape for medical device manufacturers across the globe by offering a smart, intuitive, and centralized platform that provides accurate, country-specific regulatory information. Global MedRegs is a powerful regulatory intelligence tool designed to save time, reduce compliance risks, and lower operational costs—all through a user-friendly and comprehensive interface.
Global MedRegs is your one-stop solution for accessing medical device regulatory requirements
for 100+ countries, making compliance and market access simpler, faster, and more efficient.
We help users:
We offer powerful interactive features to help users visualize and explore regulatory frameworks:
Click on a country to view its full regulatory profile.
Easily find any country or requirement, even for smaller regions.
Countries associated with MDSAP , IMDRF, ASEAN, WHO and other organisations. Countries that accept CE mark, follow ISO 13485 and many more.
Our ever-growing Resources Hub is designed to empower users with valuable content:
We value your experience!
Our Vision To be the leading global platform that empowers medical device manufacturers with accurate, up-to-date regulatory information—all in one place, saving both time and compliance costs.