IMP PHARMACEUTICAL SERVICES LIMITED – MIA(IMP) 46345
| Authorisation Number | UK MIA(IMP) 46345 |
| Category | MIA(IMP) |
| Holder | IMP PHARMACEUTICAL SERVICES LIMITED |
| Registered Address | IMP PHARMACEUTICAL SERVICES LIMITED, UNIT 23, WOODFIELDSIDE BUSINESS PARK, PENMAEN ROAD, PONTLLANFRAITH, BLACKWOOD, NP12 2DG, UNITED KINGDOM |
| Authorisation Date | Jul 21, 2025 |
| Legal Basis | InvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031] |
| Sites | 2 |
| Manufacturing Operations | 1.1 1.1.3 1.2 1.2.2 1.3 1.3.1 1.3.1.4 1.3.1.5 1.3.1.8 1.3.2 1.3.2.2 1.3.2.4 1.3.2.5 1.5 1.5.2 |
| Importation Operations | 2.2 2.2.1 2.2.1.1 2.2.1.2 2.2.2 2.2.3 2.2.3.2 2.2.3.3 2.2.3.4 2.2.3.5 2.2.3.8 2.3 2.3.1 2.3.2 2.3.4 |
| MHRA Link | View on MHRA Website |
Sites (2)
IMP PHARMACEUTICAL SERVICES LIMITED
BOTH
Country: UNITED KINGDOMProduct Class: Human Investigational Medicinal Products
Manufacturing
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.4 — Gene therapy products
1.3.1.5 — Biotechnology products
1.3.1.8 — Other biological medicinal products
1.5 — Packaging
1.5.2 — Secondary packaging
Importation
2.2 — Batch certification of imported medicinal products
2.2.1 — Sterile Products
2.2.1.1 — Aseptically prepared
2.2.1.2 — Terminally sterilised
2.2.2 — Non-sterile products
2.2.3 — Biological medicinal products
2.2.3.2 — Immunological products
2.2.3.3 — Cell therapy products
2.2.3.4 — Gene therapy products
2.2.3.8 — Other biological medicinal products
2.3 — Other Importation Activities
2.3.1 — Site of Physical Importation
2.3.2 — Importation of Intermediate which undergoes further processing
2.3.4 — Other
IMP PHARMACEUTICAL SERVICES LIMITED
BOTH
Country: UNITED KINGDOMProduct Class: Human Investigational Medicinal Products
Manufacturing
1.1 — Sterile Investigational Medicinal Products
1.1.3 — Batch certification
1.2 — Non-sterile investigational medicinal products
1.2.2 — Batch certification
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.4 — Gene therapy products
1.3.1.5 — Biotechnology products
1.3.1.8 — Other biological medicinal products
1.3.2 — Batch certification
1.3.2.2 — Immunological products
1.3.2.4 — Gene therapy products
1.3.2.5 — Biotechnology products
1.5 — Packaging
1.5.2 — Secondary packaging
Importation
2.2 — Batch certification of imported medicinal products
2.2.1 — Sterile Products
2.2.1.1 — Aseptically prepared
2.2.1.2 — Terminally sterilised
2.2.2 — Non-sterile products
2.2.3 — Biological medicinal products
2.2.3.2 — Immunological products
2.2.3.4 — Gene therapy products
2.2.3.5 — Biotechnology products
2.2.3.8 — Other biological medicinal products
2.3 — Other Importation Activities
2.3.1 — Site of Physical Importation
2.3.4 — Other
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