Suppliers / Pharmaron Manufacturing Services (UK)

Pharmaron Manufacturing Services (UK)

United Kingdom Updated 9 July 2026

Pharmaron Manufacturing Services (UK) is an API manufacturer based in United Kingdom. It holds one active US drug master file and one valid CEP. Its GMP standing is certified by US FDA and MHRA (UK). Its most recent recorded inspection, by US FDA, closed on 17 July 2025 as NAI.

1
active US DMFs
1
valid CEPs
4
registered plants 2 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 17 July 2025 NAI US FDA
  • 24 February 2022 VAI US FDA
  • 23 January 2020 VAI US FDA
  • 24 May 2018 VAI US FDA
  • 27 July 2016 VAI US FDA
  • 11 September 2015 VAI US FDA
  • 15 August 2014 VAI US FDA
  • 21 March 2012 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
CRAMLINGTON, United Kingdom Not on file
Cramlington, United Kingdom Not on file
United Kingdom, United Kingdom 3002806562
Coventry, United States 1211201

What they file, and where

Molecule Regulators Docs
Flurbiprofen EDQM, US FDA 2

Also appears on these molecule pages

Flurbiprofen API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1
MHRA (UK) None 1

Questions about Pharmaron Manufacturing Services (UK)

Does Pharmaron Manufacturing Services (UK) hold a US DMF or a CEP?
Pharmaron Manufacturing Services (UK) holds 1 active US drug master file and 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Pharmaron Manufacturing Services (UK) FDA-registered?
2 sites operated by Pharmaron Manufacturing Services (UK) carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Pharmaron Manufacturing Services (UK)'s last inspection go?
The most recent inspection on record closed on 17 July 2025 as NAI (No Action Indicated: nothing objectionable was found). 8 inspections are on file.
Where does Pharmaron Manufacturing Services (UK) manufacture?
4 registered sites are on record, in United Kingdom and United States (Cramlington, Cramlington and United Kingdom among others). Every site is listed on this page with the register it came from.
What does Pharmaron Manufacturing Services (UK) make?
1 molecule is on record against Pharmaron Manufacturing Services (UK), including Flurbiprofen. Each links through to that molecule's full manufacturer list.
Which regulators recognise Pharmaron Manufacturing Services (UK)'s GMP?
Current GMP certificates are on record from US FDA and MHRA (UK). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was NAI, on 17 July 2025.

Comparable suppliers

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates