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Simplify Complexity
- Japan regulatory access made easy
Medical Device RAC certified professional
We enable Japan regulatory access
PMDA Consultation Meeting Preparation
Marketing Authorization Application (MAA-製造販売承認申請)
STED (Summary of Technical Document) Deployment
QMS Gap Analysis
Software Life Cycle Process (JIS-T-2304)
Cybersecurity Consideration (JIS-T-81001)
National Health Insurance (NHI) Coverage Application
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