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SYMBIOSIS PHARMACEUTICAL SERVICES LIMITED – MIA(IMP) 40211

Authorisation NumberUK MIA(IMP) 40211
Category
MIA(IMP)
HolderSYMBIOSIS PHARMACEUTICAL SERVICES LIMITED
Registered AddressSYMBIOSIS PHARMACEUTICAL SERVICES LIMITED, UNIT 10, SCION HOUSE, STIRLING UNIVERSITY INNOVATION PARK, STIRLING, FK9 4NF, UNITED KINGDOM
Authorisation DateFeb 11, 2026
Legal BasisInvestigationalPart 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 [SI 2004/1031]
Sites3
Manufacturing Operations
1.1
1.1.1
1.1.1.2
1.1.1.4
1.1.1.6
1.1.3
1.2
1.2.1
1.2.1.15
1.2.2
1.3
1.3.1
1.3.1.2
1.3.1.3
1.3.1.4
1.3.1.5
1.3.1.8
1.3.2
1.3.2.2
1.3.2.4
1.3.2.5
1.3.2.8
1.4
1.4.2
1.4.2.1
1.5
1.5.2
1.6
1.6.1
1.6.2
1.6.3
1.6.4
Importation Operations
2.2
2.2.3
2.2.3.4
2.3
2.3.1
2.3.2
MHRA LinkView on MHRA Website

Sites (3)

SYMBIOSIS PHARMACEUTICAL SERVICES 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)
1.1.1.4 — Small volume liquids
1.1.1.6 — Other aseptically prepared products
1.1.3 — Batch certification
1.2 — Non-sterile investigational medicinal products
1.2.2 — Batch certification
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.2 — Immunological products
1.3.1.3 — Cell therapy products
1.3.1.4 — Gene therapy products
1.3.1.5 — Biotechnology products
1.3.1.8 — Other biological medicinal products
1.3.2 — Batch certification
1.3.2.2 — Immunological products
1.3.2.4 — Gene therapy products
1.3.2.5 — Biotechnology products
1.3.2.8 — Other biological medicinal 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
1.5 — Packaging
1.5.2 — Secondary packaging
1.6 — Quality control testing
1.6.2 — Microbiological: non-sterility
Importation
2.2 — Batch certification of imported medicinal products
2.2.3 — Biological medicinal products
2.2.3.4 — Gene therapy products
2.3 — Other Importation Activities
2.3.1 — Site of Physical Importation
2.3.2 — Importation of Intermediate which undergoes further processing
SYMBIOSIS PHARMACEUTICAL SERVICES 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
1.1.1.6 — Other aseptically prepared 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)
1.2.1.15 — Other non-sterile medicinal products
1.2.2 — Batch certification
1.3 — Biological investigational medicinal products
1.3.1 — Biological medicinal products
1.3.1.2 — Immunological products
1.3.1.4 — Gene therapy products
1.3.1.5 — Biotechnology products
1.3.1.8 — Other biological medicinal products
1.3.2 — Batch certification
1.3.2.2 — Immunological products
1.3.2.4 — Gene therapy products
1.3.2.5 — Biotechnology products
1.3.2.8 — Other biological medicinal 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
1.5 — Packaging
1.5.2 — Secondary packaging
Importation
2.2 — Batch certification of imported medicinal products
2.2.3 — Biological medicinal products
2.2.3.4 — Gene therapy products
2.3 — Other Importation Activities
2.3.1 — Site of Physical Importation
2.3.2 — Importation of Intermediate which undergoes further processing
SYMBIOSIS PHARMACEUTICAL SERVICES LIMITED
MANUFACTURING_SITE
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
1.2.2 — Batch certification
1.3 — Biological investigational medicinal products
1.3.2 — Batch certification
1.3.2.2 — Immunological products
1.3.2.4 — Gene therapy products
1.3.2.5 — Biotechnology products
1.3.2.8 — Other biological medicinal products
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

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