PMDA registration
DELPHARM DIJON
PMDA registration AG21000179 · France
Key facts
| Registration number | AG21000179 |
|---|---|
| Site | DELPHARM DIJON |
| Corporation | DELPHARM DIJON |
| Country | France |
| Type of business | Pharmaceutical foreign manufacturers |
| Registration categories | Pharmaceutical Sterile Pharmaceuticals |
| Registered | Jul 17, 2024 |
| Expires | Jul 16, 2029 |
At a glance
- 1–9 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