About regMD
AI-Powered Medical Device Regulatory Intelligence
Our Mission
regMD was built to make medical device regulatory navigation accessible to everyone — from startups bringing their first device to market to established manufacturers expanding into new jurisdictions. Understanding your regulatory pathway shouldn't require weeks of research or expensive consultants for an initial assessment.
Built by Practitioners
regMD is built by a team with deep experience in medical device regulation across ASEAN markets. We've sat on both sides of the table — as regulators and as industry operators navigating the submission process.
This tool encodes real regulatory knowledge into a classification engine that delivers results in seconds — work that typically takes days of manual research or expensive consulting engagements.
RegPath Asia
regMD is the first product from RegPath Asia — a platform designed to simplify medical device regulatory affairs across ASEAN. We're building a comprehensive suite of tools to help manufacturers navigate the complex landscape of multi-market regulatory compliance.
Disclaimer
regMD provides indicative device classifications based on AI analysis and should not be relied upon as formal regulatory advice. Classifications are approximate and intended as a starting point for your regulatory strategy. Always consult with qualified regulatory professionals and the relevant regulatory authority before making submission decisions.