Medicines and Healthcare products Regulatory Agency
| 1: Authorisation Number | UK MIA 53553 |
|---|---|
| 2: Name of authorisation holder | CENTRAL PHARMA CELL AND GENE THERAPY LTD |
| 3: Address(es) of manufacturing site(s) |
CENTRAL PHARMA CELL AND GENE THERAPY LTD, UNITS C AND D, HOMEFIELD BUSINESS PARK, HOMEFIELD ROAD, HAVERHILL, CB9 8QP, UNITED KINGDOM |
| 4: Legally registered address of authorisation holder | CENTRAL PHARMA CELL AND GENE THERAPY LTD, CAXTON ROAD, BEDFORD, MK41 0XZ, 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 | 28/12/2023 |
| 9: Annexes attached | Annex 1 and/or Annex 2 |
SCOPE OF AUTHORISATION
Annex 1
Name and address of the site:
CENTRAL PHARMA CELL AND GENE THERAPY LTD, UNITS C AND D, HOMEFIELD BUSINESS PARK, HOMEFIELD ROAD, HAVERHILL, CB9 8QP, 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 |
| [ 1.2 ] Non-sterile products |
| [ 1.2.2 ] Batch certification |
| [ 1.5 ] Packaging |
| [ 1.5.1 ] Primary packaging |
| [ 1.5.1.1 ] Capsules, hard shell |
| [ 1.5.1.2 ] Capsules, soft shell |
| [ 1.5.1.13 ] Tablets |
| [ 1.5.2 ] Secondary packaging |
| Part 2 - IMPORTATION OF MEDICINAL PRODUCTS |
| [ 2.2 ] Batch certification of imported medicinal products |
| [ 2.2.2 ] Non-sterile products |
| [ 2.3 ] Other Importation Activities |
| [ 2.3.1 ] Site of Physical Importation |
| [ 2.3.2 ] Importation of Intermediate which undergoes further processing |