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类别: REGULATORY PATHWAYS
承认(日本上市前批准)
PMDA/厚生劳动省对日本II类(无标准)、III类和IV类医疗器械的上市前批准途径。承认包括PMDA科学审评和厚劳省正式批准。
Last reviewed 2026-08-05 · Reviewed by MedFlux Editorial Board · Editorial policy
Expanded process notes below are currently maintained in English; the short definition above is localized. See our editorial policy.
WHEN IT APPLIES
Shonin is Japan’s PMDA/MHLW pre-market approval path for higher-risk devices (typically Class III/IV and some Class II without standards).
PROCESS / STEPS
- Confirm Japanese classification and pathway (Shonin vs Ninsho vs Todokede).
- Engage a DMAL holder.
- Prepare dossier and consult PMDA as needed.
- Complete review and MHLW authorization; plan PMS.
EXAMPLES
- A novel implant without a certification standard typically requires Shonin rather than Ninsho.
RELATED GUIDES & TOOLS
SOURCES
Track regulatory signals related to 承认(日本上市前批准) across 27 authorities in real time.
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