Medical Device Global Regulatory Requirements

Our mission is to facilitate global market access for medical device manufacturers by offering a user-friendly interface that navigates through country-specific regulatory requirements, ultimately saving precious time and costs.

Why choose us ?

  • One Platform, Global Reach — Access regulatory requirements from 100+ countries at your fingertips.
  • Interactive & User-Friendly — Clickable maps, comparison tables, and search options make navigation effortless.
  • Resources Hub: Access essential templates, checklists, and gap analysis tools for compliance success.

Our Team

Akash Kirani

Founder

Sowmya Arunkumar

Advisor

1k+ Satisfied users

"Global MedRegs has completely streamlined my workflow. Instead of searching across dozens of regulatory websites, | now get all the essential requirements for each country in one place. It's a game changer for regulatory professionals."

Medical Device Regulatory Affairs Specialist

"As a startup entering global markets, navigating country-specific regulations was overwhelming. Global MedRegs helped us understand classification, registration processes, and local representation rules — all in one dashboard."

CEO, Medtech Startup

"| recommend Global MedRegs to all my clients. It offers quick insights into international regulations and ensures they stay compliant as they grow globally. It's an excellent tool for consultants and large teams alike."

Regulatory Consultant

Benefits of using our platform

Save Time & Costs

Eliminate hours of regulatory research with an easy-to-use platform. Reduce Compliance Risks — Summarized regulatory requirements for easy understanding.

Empower Decision-Making

Compare regulations, identify gaps, and streamline market entry.

Resources

Access Everything You Need for Medical Device Compliance - Best Articles, Tools, ISO Standards, Templates and more

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