PMDA registration
Sysmex R&D Center Europe GmbH
PMDA registration EG21300010 · Germany
Key facts
| Registration number | EG21300010 |
|---|---|
| Site | Sysmex R&D Center Europe GmbH |
| Corporation | Sysmex R&D Center Europe GmbH |
| Country | Germany |
| Type of business | Foreign manufacturers of in vitro diagnostic drugs |
| Registration categories | In vitro diagnostic drug registration |
| Registered | Aug 4, 2025 |
| Expires | Aug 3, 2030 |
At a glance
- None PMDA inspections
- No Registration expired
- No Registration abolished
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA registered foreign manufacturers (Japan)
Foreign manufacturers of drugs and medical devices supplied to Japan must be registered (accredited) with the Ministry of Health, Labour and Welfare through the PMDA.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan