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CP PHARMACEUTICALS LIMITED – MIA(IMP) 4543

Authorisation NumberUK MIA(IMP) 4543
Category
MIA(IMP)
HolderCP PHARMACEUTICALS LIMITED
Registered AddressCP PHARMACEUTICALS LIMITED, ASH ROAD NORTH, WREXHAM, LL13 9UF, UNITED KINGDOM
Authorisation DateJul 08, 2026
Legal BasisInvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031]
Sites1
Manufacturing Operations
1.1
1.1.1
1.1.1.2
1.1.1.4
1.1.2
1.1.2.3
1.1.3
1.6
1.6.1
1.6.2
1.6.3
1.6.4
Importation Operations
2.1
2.1.1
2.1.2
2.1.3
2.1.4
2.2
2.2.1
2.2.1.1
2.2.1.2
2.2.2
2.2.3
2.2.3.5
2.2.3.6
2.3
2.3.1
MHRA LinkView on MHRA Website

Sites (2)

CP PHARMACEUTICALS LIMITED
BOTH
Country: UNITED KINGDOMProduct Class: Human Investigational Medicinal Products
Manufacturing
1.1 — Sterile Investigational Medicinal Products
1.1.1 — Aseptically prepared (processing operations for the following dosage forms)
1.1.1.2 — Lyophilisates
1.1.1.4 — Small volume liquids
1.1.2 — Terminally Sterilised (processing operations for the following dosage forms)
1.1.2.3 — Small volume liquids
1.1.3 — Batch certification
1.6 — Quality control testing
1.6.1 — Microbiological: sterility
1.6.2 — Microbiological: non-sterility
1.6.3 — Chemical/Physical
1.6.4 — Biological
Importation
2.1 — Quality control testing of imported medicinal products
2.1.1 — Microbiological: sterility
2.1.2 — Microbiological: non-sterility
2.1.3 — Chemical/Physical
2.1.4 — Biological
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
2.2.3.5 — Biotechnology products
2.2.3.6 — Human or animal extracted products
2.3 — Other Importation Activities
2.3.1 — Site of Physical Importation
CP PHARMACEUTICALS LIMITED
BOTH
Country: UNITED KINGDOMProduct Class: Human Investigational Medicinal Products
Manufacturing
1.1 — Sterile Investigational Medicinal Products
1.1.1 — Aseptically prepared (processing operations for the following dosage forms)
1.1.1.2 — Lyophilisates
1.1.1.4 — Small volume liquids
1.1.2 — Terminally Sterilised (processing operations for the following dosage forms)
1.1.2.3 — Small volume liquids
1.1.3 — Batch certification
1.6 — Quality control testing
1.6.1 — Microbiological: sterility
1.6.2 — Microbiological: non-sterility
1.6.3 — Chemical/Physical
1.6.4 — Biological
Importation
2.1 — Quality control testing of imported medicinal products
2.1.1 — Microbiological: sterility
2.1.2 — Microbiological: non-sterility
2.1.3 — Chemical/Physical
2.1.4 — Biological
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
2.2.3.5 — Biotechnology products
2.2.3.6 — Human or animal extracted products
2.3 — Other Importation Activities
2.3.1 — Site of Physical Importation

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