Medicines and Healthcare products Regulatory Agency
| 1: Authorisation Number | UK MIA(IMP) 45848 | 
|---|---|
| 2: Name of authorisation holder | QUOTIENT SCIENCES (ALNWICK) LIMITED | 
| 3: Address(es) of manufacturing site(s) | QUOTIENT SCIENCES (ALNWICK) LIMITED, TAYLOR DRIVE, ALNWICK, NE66 2DH, UNITED KINGDOM | 
| 4: Legally registered address of authorisation holder | QUOTIENT SCIENCES (ALNWICK) LIMITED, TRENT HOUSE, MERE WAY, RUDDINGTON FIELDS BUSINESS PARK, RUDDINGTON, NOTTINGHAM, NG11 6JS, UNITED KINGDOM | 
| 5: Scope of authorisation and dosage forms | ANNEX 1 and/ or ANNEX 2 | 
| 6: Legal Basis of authorisation | |
| 7: Name of responsible officer of the competent authority of the member state granting the manufacturing authorisation | Confidential | 
| 8: Authorisation Date | 09/09/2025 | 
| 9: Annexes attached | Annex 1 and/or Annex 2 | 
SCOPE OF AUTHORISATION
        Annex 2
        
          Name and address of the site: 
          
      
              
          
  
        
        
        QUOTIENT SCIENCES (ALNWICK) LIMITED, TAYLOR DRIVE, ALNWICK, NE66 2DH, UNITED KINGDOM
                                          Human Investigational Medicinal Products
                  
      | Authorised Operations | 
| MANUFACTURING OPERATIONS (according to part 1)IMPORTATION OF MEDICINAL PRODUCTS (according to part 2) | 
| Part 1 - MANUFACTURING OPERATIONS | 
| [ 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 Radiolabelled Products & Cytotoxic 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 | 
| [ 1.2.1.2 ] Capsules, soft shell | 
| [ 1.2.1.5 ] Liquids for external use | 
| [ 1.2.1.6 ] Liquids for internal use | 
| [ 1.2.1.8 ] Other solid dosage forms | 
| [ 1.2.1.11 ] Semi-solids | 
| [ 1.2.1.15 ] Other non-sterile medicinal products Radiolabelled Products & Cytotoxic Products, Moulded Tablets, Drug in a Vial, Over encapsulated product. | 
| [ 1.2.2 ] Batch certification | 
| [ 1.4 ] Other investigational medicinal products or manufacturing activitiy | 
| [ 1.4.2 ] Sterilisation of active substances/excipients/finished products: | 
| [ 1.4.2.1 ] Filtration | 
| [ 1.6 ] Quality control testing | 
| [ 1.6.1 ] Microbiological: sterility | 
| [ 1.6.2 ] Microbiological: non-sterility | 
| [ 1.6.3 ] Chemical/Physical | 
| Part 2 - IMPORTATION OF MEDICINAL PRODUCTS | 
| [ 2.1 ] Quality control testing of imported medicinal products | 
| [ 2.1.1 ] Microbiological: sterility | 
| [ 2.1.2 ] Microbiological: non-sterility | 
| [ 2.1.3 ] Chemical/Physical | 
