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PENN PHARMACEUTICAL SERVICES LIMITED – MIA(IMP) 4351

Authorisation NumberUK MIA(IMP) 4351
Category
MIA(IMP)
HolderPENN PHARMACEUTICAL SERVICES LIMITED
Registered AddressPENN PHARMACEUTICAL SERVICES LIMITED, UNITS 23-24, TAFARNAUBACH INDUSTRIAL ESTATE, TAFARNAUBACH, TREDEGAR, NP22 3AA, UNITED KINGDOM
Authorisation DateMay 13, 2026
Legal BasisInvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031]
Sites1
Manufacturing Operations
1.1
1.1.3
1.2
1.2.1
1.2.1.1
1.2.1.11
1.2.1.12
1.2.1.13
1.2.1.15
1.2.1.5
1.2.1.6
1.2.2
1.4
1.4.1
1.4.1.1
1.5
1.5.1
1.5.1.1
1.5.1.11
1.5.1.12
1.5.1.13
1.5.1.15
1.5.1.5
1.5.1.6
1.5.2
1.6
1.6.2
1.6.3
Importation Operations
2.1
2.1.2
2.1.3
2.2
2.2.1
2.2.1.1
2.2.1.2
2.2.2
2.2.3
2.2.3.1
2.2.3.2
2.2.3.5
2.2.3.6
2.3
2.3.1
2.3.2
MHRA LinkView on MHRA Website

Sites (1)

PENN 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
1.2.1 — Non-Sterile Products (processing operations for the following dosage forms)
1.2.1.1 — Capsules, hard shell
1.2.1.5 — Liquids for external use
1.2.1.6 — Liquids for internal use
1.2.1.11 — Semi-solids
1.2.1.12 — Suppositories
1.2.1.13 — Tablets
1.2.1.15 — Other non-sterile medicinal products
1.2.2 — Batch certification
1.4 — Other investigational medicinal products or manufacturing activitiy
1.4.1 — Manufacture of:
1.4.1.1 — Herbal products
1.5 — Packaging
1.5.1 — Primary packaging
1.5.1.1 — Capsules, hard shell
1.5.1.5 — Liquids for external use
1.5.1.6 — Liquids for internal use
1.5.1.11 — Semi-solids
1.5.1.12 — Suppositories
1.5.1.13 — Tablets
1.5.1.15 — Other non-sterile medicinal products
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.2 — Microbiological: non-sterility
1.6.3 — Chemical/Physical
Importation
2.1 — Quality control testing of imported medicinal products
2.1.2 — Microbiological: non-sterility
2.1.3 — Chemical/Physical
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
2.2.3.1 — Blood products
2.2.3.2 — Immunological 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
2.3.2 — Importation of Intermediate which undergoes further processing

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