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MEDPHARM LIMITED – MIA(IMP) 25076

Authorisation NumberUK MIA(IMP) 25076
Category
MIA(IMP)
HolderMEDPHARM LIMITED
Registered AddressMEDPHARM LIMITED, UNIT 1 & UNIT 3 CHANCELLOR COURT, 50 OCCAM ROAD, SURREY RESEARCH PARK, GUILDFORD, GU2 7AB, UNITED KINGDOM
Authorisation DateApr 27, 2026
Legal BasisInvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031]
Sites1
Manufacturing Operations
1.2
1.2.1
1.2.1.11
1.2.1.12
1.2.1.14
1.2.1.4
1.2.1.5
1.2.1.6
1.2.1.8
1.2.1.9
1.2.2
1.5
1.5.1
1.5.1.11
1.5.1.12
1.5.1.14
1.5.1.4
1.5.1.5
1.5.1.6
1.5.1.8
1.5.1.9
1.5.2
1.6
1.6.2
1.6.3
Importation Operations
2.1
2.1.2
2.1.3
2.2
2.2.2
MHRA LinkView on MHRA Website

Sites (1)

MEDPHARM LIMITED
BOTH
Country: UNITED KINGDOMProduct Class: Human Investigational Medicinal Products
Manufacturing
1.2 — Non-sterile investigational medicinal products
1.2.1 — Non-Sterile Products (processing operations for the following dosage forms)
1.2.1.4 — Impregnated matrices
1.2.1.5 — Liquids for external use
1.2.1.6 — Liquids for internal use
1.2.1.8 — Other solid dosage forms
1.2.1.9 — Pressurised preparations
1.2.1.11 — Semi-solids
1.2.1.12 — Suppositories
1.2.1.14 — Transdermal patches
1.2.2 — Batch certification
1.5 — Packaging
1.5.1 — Primary packaging
1.5.1.4 — Impregnated matrices
1.5.1.5 — Liquids for external use
1.5.1.6 — Liquids for internal use
1.5.1.8 — Other solid dosage forms
1.5.1.9 — Pressurised preparations
1.5.1.11 — Semi-solids
1.5.1.12 — Suppositories
1.5.1.14 — Transdermal patches
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
2.2.2 — Non-sterile products

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