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Support for development of medical devices
Analysis of image for medical use
Support for entry into foreign markets
Support for entry into Japanese markets
Revision of the Pharmaceutical Affairs Law
To support updating Marketing Approval Application File
Support for development of new medical technologies
Monitoring
QC
DM/Statistical analysis
GCP Audit
Medical writing
Sending Clinical Research Specialists
Application and registration of approvals and licenses
Medical Device Track record in obtaining approval of
Case study
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