Regulatory document
Handling of Situations requiring submission of “Documents related to Clinical Study…
PMDA · Information · Japan
Key facts
| Title | Handling of Situations requiring submission of “Documents related to Clinical Study Results” for Medical Devices (Responses based on Measures across Pre-and Post-Marketing Phases) |
|---|---|
| Issuer | Pharmaceuticals and Medical Devices Agency |
| Source | PMDA |
| Document type | Information |
| Country or region | Japan |
| Document | pmda.go.jp |
| Issuer website | pmda.go.jp |
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