Uk Mhra Gmp
THORNTON & ROSS LIMITEDTHORNTON & ROSS LIMITED – UK MHRA GMP Certificate UK MIA 240 Insp GMP 240/14497-0035[H]
Record Details
This Uk Mhra Gmp record concerns THORNTON & ROSS LIMITED, with an inspection on April 24, 2025, issued by the MHRA, covering drugs.
- Company
- THORNTON & ROSS LIMITED
- Compliance status
- GMPC
- Certificate type
- GMP
- Inspection date
- April 24, 2025
- Issued
- April 25, 2025
- MIA number
- UK MIA 240
- Site address
- MANCHESTER ROAD, LINTHWAITE, HUDDERSFIELD, HD7 5QH, UNITED KINGDOM
- Country
- UNITED KINGDOM
- Products
- Human Medicinal Products
- Manufacturing operations
- 1. MANUFACTURING OPERATIONS [ 1.1 ] Sterile Products [ 1.1.3 ] Batch certification [ 1.2 ] Non-sterile products [ 1.2.1 ] Non-Sterile Products (processing operations for the following dosage forms) [ 1.2.1.5 ] Liquids for external use [ 1.2.1.6 ] Liquids for internal use [ 1.2.1.11 ] Semi-solids [ 1.2.1.12 ] Suppositories [ 1.2.1.17 ] Other non-sterile medicinal productsCreams, ointments, ear drops, nasal drops, solutions, suspensions, emulsions and lotions. Medical Devices. [ 1.2.2 ] Batch certification [ 1.4 ] Other products or manufacturing activity [ 1.4.1 ] Manufacture of: [ 1.4.1.1 ] Herbal products [ 1.4.1.3 ] OtherMedical Devices [ 1.5 ] Packaging [ 1.5.1 ] Primary packaging [ 1.5.1.1 ] Capsules, hard shell [ 1.5.1.2 ] Capsules, soft shell [ 1.5.1.5 ] Liquids for external use [ 1.5.1.6 ] Liquids for internal use [ 1.5.1.8 ] Other solid dosage forms [ 1.5.1.11 ] Semi-solids [ 1.5.1.12 ] Suppositories [ 1.5.1.13 ] Tablets [ 1.5.1.17 ] Other non-sterile medicinal productsCreams, ointments, ear drops, nasal drops, solutions, suspensions, emulsions and lotions. Medical Devices [ 1.5.2 ] Secondary packaging [ 1.6 ] Quality control testing [ 1.6.2 ] Microbiological: non-sterility [ 1.6.3 ] Chemical/Physical 2. IMPORTATION OF MEDICINAL PRODUCTS [ 2.1 ] Quality control testing of imported medicinal products [ 2.1.2 ] Microbiological: non-sterility [ 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 [ 2.3.4 ] OtherMedical Devices
- 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 · 4a30fea8-d09b-4dd3-903a-aecfa84a8fcd
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