PMDA registration
Randox Laboratories Ltd.-What
PMDA registration EG20500020 · U.K.
Key facts
| Registration number | EG20500020 |
|---|---|
| Site | Randox Laboratories Ltd.-What |
| Corporation | Randox Laboratories Ltd. |
| Country | U.K. |
| Type of business | Foreign manufacturers of in vitro diagnostic drugs |
| Registration categories | In vitro diagnostic drug registration |
| Registered | Nov 21, 2023 |
| Expires | Nov 20, 2028 |
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