Uk Mhra Gmp
PHARMARON UK LIMITEDPHARMARON UK LIMITED – UK MHRA GMP Certificate UK MIA(IMP) 47794 Insp IMP 47794/21159709-0004[I]
Record Details
This Uk Mhra Gmp record concerns PHARMARON UK LIMITED, with an inspection on October 21, 2025, issued by the MHRA, covering drugs.
- Company
- PHARMARON UK LIMITED
- Compliance status
- GMPC
- Certificate type
- IMP
- Inspection date
- October 21, 2025
- Issued
- November 14, 2025
- MIA number
- UK MIA(IMP) 47794
- Site address
- WEST HILL INNOVATION PARK, HERTFORD ROAD, HODDESDON, EN11 9FH, 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 [ 1.2.1 ] Non-Sterile Products (processing operations for the following dosage forms) [ 1.2.1.1 ] Capsules, hard shell [ 1.2.1.8 ] Other solid dosage formsPowders and granules [ 1.2.1.13 ] Tablets [ 1.2.2 ] Batch certification [ 1.5 ] Packaging [ 1.5.1 ] Primary packaging [ 1.5.1.1 ] Capsules, hard shell [ 1.5.1.8 ] Other solid dosage formsPowders and granules [ 1.5.1.13 ] Tablets [ 1.6 ] Quality control testing [ 1.6.3 ] Chemical/Physical 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 [ 2.2.1 ] Sterile Products [ 2.2.1.1 ] Aseptically prepared [ 2.2.1.2 ] Terminally sterilised [ 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 [ 2.3.4 ] Other Importation of QP certified IMPs from a country on the 'approved country for import list'
- Restrictions
- Packaging operations for IMPs performed at this site are for Open-Label studies only. 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 · 8ec55bd8-5226-418d-b6ea-404145619a21
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