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ALLERGY THERAPEUTICS (UK) LIMITED – MIA(IMP) 17087

Authorisation NumberUK MIA(IMP) 17087
Category
MIA(IMP)
HolderALLERGY THERAPEUTICS (UK) LIMITED
Registered AddressALLERGY THERAPEUTICS (UK) LIMITED, DOMINION WAY, WORTHING, Data Not Available, WEST SUSSEX, BN14 8SA, UNITED KINGDOM
Authorisation DateFeb 17, 2026
Legal BasisInvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031]
Sites2
Manufacturing Operations
1.1
1.1.1
1.1.1.2
1.1.1.4
1.1.3
1.2
1.2.1
1.2.1.15
1.2.1.6
1.2.2
1.3
1.3.1
1.3.1.1
1.3.1.2
1.3.2
1.3.2.1
1.3.2.2
1.4
1.4.2
1.4.2.1
1.4.2.2
1.4.2.3
1.5
1.5.1
1.5.1.13
1.5.1.15
1.5.1.5
1.5.1.6
1.5.1.8
1.5.2
1.6
1.6.1
1.6.2
1.6.3
1.6.4
MHRA LinkView on MHRA Website

Sites (2)

ALLERGY THERAPEUTICS 2
MANUFACTURING_SITE
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
1.2 — Non-sterile investigational medicinal products
1.2.1 — Non-Sterile Products (processing operations for the following dosage forms)
1.2.1.6 — Liquids for internal use
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.1 — Blood products
1.3.1.2 — Immunological products
1.4 — Other investigational medicinal products or manufacturing activitiy
1.4.2 — Sterilisation of active substances/excipients/finished products:
1.4.2.1 — Filtration
1.4.2.2 — Dry heat
1.4.2.3 — Moist heat
1.5 — Packaging
1.5.1 — Primary packaging
1.5.1.5 — Liquids for external use
1.5.1.8 — Other solid dosage forms
1.5.1.13 — Tablets
1.5.1.15 — Other non-sterile medicinal products
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.1 — Microbiological: sterility
1.6.2 — Microbiological: non-sterility
1.6.3 — Chemical/Physical
1.6.4 — Biological
ALLERGY THERAPEUTICS (UK) LIMITED
MANUFACTURING_SITE
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
1.1.3 — Batch certification
1.2 — Non-sterile investigational medicinal products
1.2.1 — Non-Sterile Products (processing operations for the following dosage forms)
1.2.1.6 — Liquids for internal use
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
1.3.1.1 — Blood products
1.3.1.2 — Immunological products
1.3.2 — Batch certification
1.3.2.1 — Blood products
1.3.2.2 — Immunological products
1.4 — Other investigational medicinal products or manufacturing activitiy
1.4.2 — Sterilisation of active substances/excipients/finished products:
1.4.2.1 — Filtration
1.4.2.2 — Dry heat
1.4.2.3 — Moist heat
1.5 — Packaging
1.5.1 — Primary packaging
1.5.1.5 — Liquids for external use
1.5.1.6 — Liquids for internal use
1.5.1.8 — Other solid dosage forms
1.5.1.13 — Tablets
1.5.1.15 — Other non-sterile medicinal products
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.1 — Microbiological: sterility
1.6.3 — Chemical/Physical
1.6.4 — Biological

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