Medicines and Healthcare products Regulatory Agency
| 1: Authorisation Number | UK MIA(IMP) 13485 | 
|---|---|
| 2: Name of authorisation holder | MW ENCAP LIMITED | 
| 3: Address(es) of manufacturing site(s) | MW ENCAP LIMITED, UNITS 1-8, OAKBANK PARK WAY, OAKBANK INDUSTRIAL ESTATE, MID CALDER, LIVINGSTON, EH53 0TH, UNITED KINGDOM | 
| 4: Legally registered address of authorisation holder | MW ENCAP LIMITED, UNITS 1-8, OAKBANK PARK WAY, OAKBANK INDUSTRIAL ESTATE, MID CALDER, LIVINGSTON, EH53 0TH, 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 | 24/10/2025 | 
| 9: Annexes attached | Annex 1 and/or Annex 2 | 
SCOPE OF AUTHORISATION
        Annex 2
        
          Name and address of the site: 
          
      
              
          
  
        
        
        MW ENCAP LIMITED, UNITS 1-8, OAKBANK PARK WAY, OAKBANK INDUSTRIAL ESTATE, MID CALDER, LIVINGSTON, EH53 0TH, 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 | 
| [ 1.2 ] 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 | 
| [ 1.2.1.15 ] Other non-sterile medicinal products Liquid fill capsules of Cytotoxics. Packing for open labelled clinical studies only (no blinding) | 
| [ 1.3 ] Biological investigational medicinal products | 
| [ 1.3.1 ] Biological medicinal products | 
| [ 1.3.1.5 ] Biotechnology products | 
| [ 1.3.1.6 ] Human or animal extracted 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 Liquid fill capsules of Cytotoxics | 
| [ 1.5.2 ] Secondary packaging | 
| [ 1.6 ] Quality control testing | 
| [ 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 | 
| [ 2.1.3 ] Chemical/Physical | 
| [ 2.2 ] Batch certification of imported medicinal products | 
| [ 2.2.2 ] Non-sterile products | 
| [ 2.3 ] Other Importation Activities | 
| [ 2.3.2 ] Importation of Intermediate which undergoes further processing | 
| [ 2.3.4 ] Other Importation of QP certified IMPs from a country on the approved country for import list | 
