PMDA registration
Sandoz GmbH - Betriebssta( ̈)tte / Manufacturing Site Drug Substance Kundl (DSK)
PMDA registration AG22500010 · Austria
Key facts
| Registration number | AG22500010 |
|---|---|
| Site | Sandoz GmbH - Betriebssta( ̈)tte / Manufacturing Site Drug Substance Kundl (DSK) |
| Corporation | Sandoz GmbH |
| Country | Austria |
| Type of business | Pharmaceutical foreign manufacturers |
| Registration categories | Pharmaceuticals, biological products, etc. |
| Registered | Apr 22, 2023 |
| Expires | Apr 21, 2028 |
At a glance
- None PMDA inspections
- No Registration expired
- Yes 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