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UPPERTON LIMITED – MIA(IMP) 49934

Authorisation NumberUK MIA(IMP) 49934
Category
MIA(IMP)
HolderUPPERTON LIMITED
Registered AddressUPPERTON LIMITED, ALBERT EINSTEIN CENTRE, NOTTINGHAM SCIENCE AND TECHNOLOGY PARK, NOTTINGHAM, NG7 2TN, UNITED KINGDOM
Authorisation DateDec 22, 2025
Legal BasisInvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031]
Sites2
Manufacturing Operations
1.2
1.2.1
1.2.1.1
1.2.1.11
1.2.1.13
1.2.1.15
1.2.1.6
1.2.1.8
1.2.2
1.3
1.3.1
1.3.1.8
1.3.2
1.3.2.8
1.4
1.4.1
1.4.1.1
1.5
1.5.1
1.5.1.1
1.5.1.11
1.5.1.13
1.5.1.15
1.5.1.6
1.5.1.8
1.5.2
1.6
1.6.3
1.6.4
MHRA LinkView on MHRA Website

Sites (2)

UPPERTON LIMITED
MANUFACTURING_SITE
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)
1.2.1.1 — Capsules, hard shell
1.2.1.6 — Liquids for internal use
1.2.1.8 — Other solid dosage forms
1.2.1.11 — Semi-solids
1.2.1.13 — Tablets
1.2.1.15 — Other non-sterile medicinal products
1.2.2 — Batch certification
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.8 — Other biological medicinal products
1.3.2 — Batch certification
1.3.2.8 — Other biological medicinal products
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
1.5.1.6 — Liquids for internal use
1.5.1.8 — Other solid dosage forms
1.5.1.11 — Semi-solids
1.5.1.13 — Tablets
1.5.1.15 — Other non-sterile medicinal products
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.3 — Chemical/Physical
1.6.4 — Biological
UPPERTON LIMITED
MANUFACTURING_SITE
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)
1.2.1.1 — Capsules, hard shell
1.2.1.6 — Liquids for internal use
1.2.1.8 — Other solid dosage forms
1.2.1.11 — Semi-solids
1.2.1.13 — Tablets
1.2.1.15 — Other non-sterile medicinal products
1.2.2 — Batch certification
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.8 — Other biological medicinal products
1.3.2 — Batch certification
1.3.2.8 — Other biological medicinal products
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
1.5.1.6 — Liquids for internal use
1.5.1.8 — Other solid dosage forms
1.5.1.11 — Semi-solids
1.5.1.13 — Tablets
1.5.1.15 — Other non-sterile medicinal products
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.3 — Chemical/Physical
1.6.4 — Biological

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