PMDA inspection
Shilpa Pharma Lifesciences Limited Unit-1
PMDA inspection 5130508025325 · India · Suitable
Key facts
| Control number | 5130508025325 |
|---|---|
| Manufacturing site | Shilpa Pharma Lifesciences Limited Unit-1 |
| Location | Plot No.1A&1A‘P', 1B, 2, 2A, 2B, 3A to 3E, 4A, 5A, 4B&5B, Deosugur Industrial Area, Deosugur-584 170, Raichur District, Karnataka, In |
| Country | India |
| Product type | Pharmaceuticals |
| Application type | Complete Change |
| Inspection method | Remote |
| Inspection month | Dec 1, 2023 |
| Result | Suitable |
| Result notified | Jan 4, 2024 |
| PMDA registration | AG12300410 |
About PMDA GMP inspections (Japan)
Japan's PMDA conducts GMP and QMS inspections of domestic and foreign manufacturing sites that supply the Japanese market.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan