Medicines and Healthcare products Regulatory Agency
WHOLESALE DISTRIBUTION AUTHORISATION
(MEDICINAL PRODUCTS FOR HUMAN USE)
1. Authorisation Number | UK WDA(H) 101 |
2. Name of Authorisation Holder | NOVARTIS PHARMACEUTICALS UK LIMITED |
3. Legally registered address of Authorisation Holder | NOVARTIS PHARMACEUTICALS UK LIMITED, 2ND FLOOR, THE WEST WORKS BUILDING, WHITE CITY PLACE, 195 WOOD LANE, LONDON, W12 7FQ, UNITED KINGDOM |
4. Address(es) of Site(s) |
NOVARTIS PHARMACEUTICALS UK LIMITED, 2ND FLOOR, THE WEST WORKS BUILDING, WHITE CITY PLACE, 195 WOOD LANE, LONDON, W12 7FQ, UNITED KINGDOM |
5. Scope of authorisation (complete for each site under 4) | ANNEX 1 |
6. Legal basis of authorisation | Regulation 18 of the Human Medicines Regulations 2012 |
7. Name of responsible officer of the competent authority of the member state granting the wholesaling authorisation | Confidential |
8. Date | 06/11/2024 |
9. Annexes attached | Annex 1 Scope of wholesale distribution authorisation
Annex 2 (Optional) Address(es) of contract wholesale distribution sites and their authorisation number
Annex 3 (Optional) Name(s) of responsible person(s)
Annex 4 (Optional) Date of Inspection on which authorisation was granted
Annex 5 Additional provisions |
ANNEX 1
Name and address of the site:
NOVARTIS PHARMACEUTICALS UK LIMITED, 2ND FLOOR, THE WEST WORKS BUILDING, WHITE CITY PLACE, 195 WOOD LANE, LONDON, W12 7FQ, UNITED KINGDOM
1. MEDICINAL PRODUCTS |
1.1 With “an authorisation” (a UK, Great Britain or Northern Ireland Marketing Authorisation, an Article 126a authorisation, a certificate of registration or traditional herbal registration) |
1.2 Without “an authorisation” (a UK, Great Britain or Northern Ireland Marketing Authorisation, an Article 126a authorisation, a certificate of registration or traditional herbal registration) in GB or EEA and intended for the UK market |
2. AUTHORISED WHOLESALE DISTRIBUTION OPERATIONS |
2.1 Procurement |
2.3 Supply |
2.4 Export |
2.6 Products imported from countries on a list |
2.6a Products certified under Article 51 of Directive 2001/83/EC |
2.6b Products not certified under Article 51 of Directive 2001/83/EC |
3. MEDICINAL PRODUCTS WITH ADDITIONAL REQUIREMENTS |
3.1.2 Medicinal products derived from blood |
3.1.3 Immunological medicinal products |
3.1.4 Radiopharmaceutical (including radionuclide kits) |
3.3 Cold chain products (requiring low temperature handling) |
3.4 Other ProductsProducts in the category Advanced Therapy Medicinal Product (ATMP) |
Any restrictions or clarifying remarks (for all users)
4 Categories of Products Handled at this Site: 4.1 Prescription Only Medicines, 4.2 General Sales List, 4.4 Pharmacy