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Uk Mhra Gmp
•COURTIN & WARNER LIMITED•October 1, 2025

COURTIN & WARNER LIMITED – UK MHRA GMP Certificate UK API 24 Insp GMP 24/18490046-0004

Record Details

This Uk Mhra Gmp record concerns COURTIN & WARNER LIMITED, with an inspection on October 1, 2025, issued by the MHRA, covering drugs.

Company
COURTIN & WARNER LIMITED
Compliance status
GMPC
Certificate type
GMP
Inspection date
October 1, 2025
Issued
January 2, 2026
MIA number
UK API 24
Site address
UNIT F, MALLING BROOKS, BROOKS ROAD, LEWES, BN7 2QG, UNITED KINGDOM
Country
UNITED KINGDOM
Products
Human Medicinal Products
Manufacturing operations
[4000007414] PHENOBARBITONE SODIUM [1000002667] ETHAMBUTOL [1000009661] NYSTATIN [1000007380] GABAPENTIN [1000008543] LORAZEPAM [2000008271] CAFFEINE CITRATE [1000009411] SUCRALFATE [1000001509] CAFFEINE AND SODIUM BENZOATE Active Substances 3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES PHENOBARBITONE SODIUM 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.4  Other Repacker 3.5 General Finishing Steps 3.5.1  Physical Processing Steps Re-packer 3.5.2  Primary Packaging 3.5.3  Secondary Packaging ETHAMBUTOL 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.4  Other Re-packer 3.5 General Finishing Steps 3.5.1  Physical Processing Steps Repacking 3.5.2  Primary Packaging 3.5.3  Secondary Packaging NYSTATIN 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.4  Other Re-packer 3.5 General Finishing Steps 3.5.1  Physical Processing Steps Re-packer 3.5.2  Primary Packaging 3.5.3  Secondary Packaging GABAPENTIN 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.4  Other Re-packer 3.5 General Finishing Steps 3.5.1  Physical Processing Steps Re-packer 3.5.2  Primary Packaging 3.5.3  Secondary Packaging LORAZEPAM 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.4  Other Re-packer 3.5 General Finishing Steps 3.5.1  Physical Processing Steps Repacker 3.5.2  Primary Packaging 3.5.3  Secondary Packaging CAFFEINE CITRATE 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.1  Manufacture Of Active Substance Intermediates 3.1.2  Manufacture Of Crude Active Substance 3.5 General Finishing Steps 3.5.2  Primary Packaging 3.5.3  Secondary Packaging 3.6 Quality Control Testing 3.6.1  Physical / Chemical testing SUCRALFATE 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.4  Other Re-packer 3.5 General Finishing Steps 3.5.1  Physical Processing Steps Repacker 3.5.2  Primary Packaging 3.5.3  Secondary Packaging CAFFEINE AND SODIUM BENZOATE 3.1 Manufacture of Active Substance by Chemical Synthesis 3.1.1  Manufacture Of Active Substance Intermediates 3.1.2  Manufacture Of Crude Active Substance 3.5 General Finishing Steps 3.5.2  Primary Packaging 3.5.3  Secondary Packaging 3.6 Quality Control Testing 3.6.1  Physical / Chemical testing
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 · 7a79aedf-988a-415f-b569-71cf68bb7b19

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
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