Uk Mhra Gmp
PHARMARON BIOLOGICS (UK) LTDPHARMARON BIOLOGICS (UK) LTD – UK MHRA GMP Certificate UK MIA(IMP) 30013 Insp GMP/IMP 30013/311656-0008[I]
Record Details
This Uk Mhra Gmp record concerns PHARMARON BIOLOGICS (UK) LTD, with an inspection on January 30, 2025, issued by the MHRA, covering biologics.
- Company
- PHARMARON BIOLOGICS (UK) LTD
- Compliance status
- GMPC
- Certificate type
- GMP/IMP
- Inspection date
- January 30, 2025
- Issued
- January 30, 2025
- MIA number
- UK MIA(IMP) 30013
- Site address
- NATIONAL BIOMANUFACTURING CENTRE, ESTUARY BANKS, ESTUARY COMMERCE PARK, SPEKE ROAD, LIVERPOOL, L24 8RB, UNITED KINGDOM
- Country
- UNITED KINGDOM
- Products
- Human Investigational Medicinal Products
- Manufacturing operations
- 1. MANUFACTURING OPERATIONS [ 1.1 ] Sterile Investigational Medicinal Products [ 1.1.3 ] Batch certification [ 1.2 ] Non-sterile investigational medicinal products [ 1.2.2 ] Batch certification [ 1.3 ] Biological investigational medicinal products [ 1.3.1 ] Biological medicinal products [ 1.3.1.2 ] Immunological products [ 1.3.1.3 ] Cell therapy products [ 1.3.1.4 ] Gene therapy products [ 1.3.1.5 ] Biotechnology products [ 1.3.1.6 ] Human or animal extracted products [ 1.3.1.8 ] Other biological medicinal productsBiological Active Starting Materials [ 1.6 ] Quality control testing [ 1.6.2 ] Microbiological: non-sterility [ 1.6.3 ] Chemical/Physical [ 1.6.4 ] Biological 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 [ 2.2.3 ] Biological medicinal products [ 2.2.3.2 ] Immunological products [ 2.2.3.3 ] Cell therapy products [ 2.2.3.4 ] Gene therapy products [ 2.2.3.5 ] Biotechnology products [ 2.2.3.6 ] Human or animal extracted products [ 2.2.3.8 ] Other biological medicinal productsBiological Active Starting Materials
- Restrictions
- This certificate is issued based on a desk-based assessment of GMP compliance information provided by the manufacturer. This certificate should be used in combination with the relevant authorisation/registration. A risk-based site inspection programme remains in force.
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ID · 4333f9d5-cb7d-4ab8-8f84-182cf5786ac0
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