Suppliers / Brunel Healthcare Manufacturing

Brunel Healthcare Manufacturing

United Kingdom Updated 9 July 2026

Brunel Healthcare Manufacturing is a finished-dose manufacturer based in United Kingdom. It appears in 31 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, EDE (AE) and EEC_EAEU. Its GMP standing is certified by MHRA (UK).

0
active US DMFs
0
valid CEPs
4
registered plants
31
filings across 4 regulators

Registered plants

Site FDA FEI
Swadlincote, United Arab Emirates Not on file
Derby, United Arab Emirates Not on file
SWADLINCOTE, United Kingdom Not on file
SWADLINCOTE, United Kingdom Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 19 None
EDE (AE) 9 None
EEC_EAEU 2 None
JFDA (JO) 1 None
MHRA (UK) None 4

Questions about Brunel Healthcare Manufacturing

Does Brunel Healthcare Manufacturing hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Brunel Healthcare Manufacturing. It does have 31 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Brunel Healthcare Manufacturing manufacture?
4 registered sites are on record, in United Arab Emirates and United Kingdom (Swadlincote, Derby and Swadlincote among others). Every site is listed on this page with the register it came from.
Which regulators recognise Brunel Healthcare Manufacturing's GMP?
Current GMP certificates are on record from 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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Comparable suppliers

ALMAC Pharma Services also in United Kingdom Almac Sciences also in United Kingdom AstraZeneca UK also in United Kingdom Bard Pharmaceuticals also in United Kingdom Bell, Sons & Co (Druggists) also in United Kingdom

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