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RAPath

RAPath

Medical Device Regulatory Reference โ€” Plain English. Properly sourced.

RAPath is an open, community-maintained reference for medical device regulation across 16+ jurisdictions. Every page is written in plain English, links back to the authoritative legislative or regulatory source, and is openly available to anyone who needs it.

๐ŸŒ rapath.github.io


Live Sites

Jurisdiction Regulator Status URL
๐Ÿ‡ฆ๐Ÿ‡บ Australia TGA Live rapath.github.io/au
๐Ÿ‡ช๐Ÿ‡บ European Union MDR & IVDR Live rapath.github.io/eu
๐Ÿ‡จ๐Ÿ‡ฆ Canada Health Canada Live rapath.github.io/hc
๐Ÿ‡ธ๐Ÿ‡ฌ Singapore HSA Live rapath.github.io/sg
๐Ÿ‡ฌ๐Ÿ‡ง United Kingdom MHRA Live rapath.github.io/uk
๐Ÿ‡บ๐Ÿ‡ธ United States FDA Live rapath.github.io/us
๐Ÿ‡ฏ๐Ÿ‡ต Japan PMDA Live rapath.github.io/jp
๐Ÿ‡จ๐Ÿ‡ญ Switzerland Swissmedic Live rapath.github.io/swiss
๐Ÿ‡จ๐Ÿ‡ณ China NMPA Live rapath.github.io/cn
๐Ÿ‡ฎ๐Ÿ‡ณ India CDSCO Live rapath.github.io/in
๐Ÿ‡ฐ๐Ÿ‡ท South Korea MFDS Live rapath.github.io/kr
๐Ÿ‡ง๐Ÿ‡ท Brazil ANVISA Lives rapath.github.io/br
๐Ÿ‡ฒ๐Ÿ‡พ Malaysia MDA Live rapath.github.io/my
๐Ÿ‡ฎ๐Ÿ‡ฉ Indonesia BPOM Live rapath.github.io/id
๐Ÿ‡ป๐Ÿ‡ณ Vietnam DAV / MOH Live rapath.github.io/vt
๐Ÿ‡ท๐Ÿ‡บ Russia Roszdravnadzor In progress rapath.github.io/ru

What RAPath Is

Regulatory frameworks for medical devices are accurate but difficult to navigate. Legislation is authoritative but hard to read. Official guidance is comprehensive but scattered across multiple sources.

RAPath sits between official sources and the reader โ€” structured, searchable, and plain English โ€” with every page linked back to the authoritative legislative or regulatory source. It is not a replacement for official regulatory sources. It is a navigation aid.

RAPath is for:

  • Regulatory affairs professionals and consultants
  • Sponsors and manufacturers entering new markets
  • Importers and distributors
  • Anyone new to medical device regulation in any of the covered jurisdictions

How to Contribute

RAPath is a community reference. Regulatory affairs professionals who flag errors, suggest improvements, or contribute content make this resource better for everyone.


Disclaimer

โš ๏ธ Content across all RAPath sites is written with AI assistance and is intended as a navigation aid only. Always verify against official regulatory sources before making any regulatory decisions. RAPath is not affiliated with any regulatory authority. Nothing on this site constitutes legal or regulatory advice.


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Last updated: May 2026

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    RAPath Global Hub - Medical Device Regulatory Reference in Plain English. Properly sourced.

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