Medicines and Healthcare products Regulatory Agency
| 1: Authorisation Number | UK MIA 530 | 
|---|---|
| 2: Name of authorisation holder | NORTON HEALTHCARE LIMITED | 
| 3: Address(es) of manufacturing site(s) | NORTON HEALTHCARE LIMITED T\A IVAX PHARMACEUTICALS UK, ASTON LANE NORTH, WHITEHOUSE VALE INDUSTRIAL ESTATE, RUNCORN, WA7 3FA, UNITED KINGDOM | 
| 4: Legally registered address of authorisation holder | NORTON HEALTHCARE LIMITED, RIDINGS POINT, WHISTLER DRIVE, CASTLEFORD, WF10 5HX, 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 | 18/09/2025 | 
| 9: Annexes attached | Annex 1 and/or Annex 2 | 
SCOPE OF AUTHORISATION
        Annex 1
        
          Name and address of the site: 
          
      
              
          
  
        
        
        NORTON HEALTHCARE LIMITED T\A IVAX PHARMACEUTICALS UK, ASTON LANE NORTH, WHITEHOUSE VALE INDUSTRIAL ESTATE, RUNCORN, WA7 3FA, UNITED KINGDOM
                                Human 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 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 Suspension and Emulsion Products | 
| [ 1.1.3 ] Batch certification | 
| [ 1.3 ] Biological medicinal products | 
| [ 1.3.1 ] Biological medicinal products | 
| [ 1.3.1.8 ] Other biological medicinal products Monoclonal Antibodies | 
| [ 1.3.2 ] Batch certification | 
| [ 1.3.2.8 ] Other biological medicinal products Monoclonal Antibodies | 
| [ 1.4 ] Other products or manufacturing activity | 
| [ 1.4.2 ] Sterilisation of active substances/excipients/finished products: | 
| [ 1.4.2.1 ] Filtration | 
| [ 1.4.2.3 ] Moist heat | 
| [ 1.5 ] Packaging | 
| [ 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 | 
| Part 2 - IMPORTATION OF MEDICINAL PRODUCTS | 
| [ 2.1 ] Quality control testing of imported medicinal products | 
| [ 2.1.1 ] Microbiological: sterility | 
| [ 2.1.3 ] Chemical/Physical | 
| [ 2.1.4 ] Biological | 
| [ 2.2 ] Batch certification of imported medicinal products | 
| [ 2.2.1 ] Sterile Products | 
| [ 2.2.1.1 ] Aseptically prepared | 
| [ 2.2.1.2 ] Terminally sterilised | 
| [ 2.2.2 ] Non-sterile products | 
| [ 2.2.3 ] Biological medicinal products | 
| [ 2.2.3.8 ] Other biological medicinal products Monoclonal Antibodies | 
| [ 2.3 ] Other Importation Activities | 
| [ 2.3.1 ] Site of Physical Importation | 
| [ 2.3.2 ] Importation of Intermediate which undergoes further processing | 
