PMDA registration
Fujirebio Diagnostics AB
PMDA registration EG20380022 · Sweden
Key facts
| Registration number | EG20380022 |
|---|---|
| Site | Fujirebio Diagnostics AB |
| Corporation | Fujirebio Diagnostics AB |
| Country | Sweden |
| Type of business | Foreign manufacturers of in vitro diagnostic drugs |
| Registration categories | In vitro diagnostic drug registration |
| Registered | Jun 11, 2017 |
| Expires | Jun 10, 2022 |
At a glance
- None PMDA inspections
- Yes 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