Medicines and Healthcare products Regulatory Agency
| 1: Authorisation Number | UK MIA 25258 |
|---|---|
| 2: Name of authorisation holder | GLENMARK PHARMACEUTICALS EUROPE LIMITED |
| 3: Address(es) of manufacturing site(s) |
GLENMARK PHARMACEUTICALS EUROPE LIMITED , BUILDING 2, CROXLEY GREEN BUSINESS PARK, MARLINS MEADOW, WATFORD, WD18 8YA, UNITED KINGDOM |
| 4: Legally registered address of authorisation holder | GLENMARK PHARMACEUTICALS EUROPE LIMITED, LAXMI HOUSE, 2-B DRAYCOTT AVENUE, KENTON, HARROW, HA3 0BU, 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 | 14/03/2024 |
| 9: Annexes attached | Annex 1 and/or Annex 2 |
SCOPE OF AUTHORISATION
Annex 1
Name and address of the site:
GLENMARK PHARMACEUTICALS EUROPE LIMITED , BUILDING 2, CROXLEY GREEN BUSINESS PARK, MARLINS MEADOW, WATFORD, WD18 8YA, 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 |
| Part 2 - IMPORTATION OF MEDICINAL PRODUCTS |
| [ 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 |