Suppliers / Bard Pharmaceuticals

Bard Pharmaceuticals

United Kingdom Updated 9 July 2026

Bard Pharmaceuticals is a finished-dose manufacturer based in United Kingdom. It appears in 30 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with NPRA (MY), EDE (AE) and Health Canada. Its GMP standing is certified by MHRA (UK) and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
2
registered plants
30
filings across 6 regulators

Registered plants

Site FDA FEI
CAMBRIDGE, United Arab Emirates Not on file
CAMBRIDGE, United Kingdom Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 9 None
EDE (AE) 8 None
Health Canada 5 None
ARCSA (EC) 4 None
MINSA (CR) 3 None
DAV (Vietnam) 1 None
MHRA (UK) None 4
ANVISA (Brazil) None 2

Questions about Bard Pharmaceuticals

Does Bard Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bard Pharmaceuticals. It does have 30 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Bard Pharmaceuticals manufacture?
2 registered sites are on record, in United Arab Emirates and United Kingdom (Cambridge among others). Every site is listed on this page with the register it came from.
Which regulators recognise Bard Pharmaceuticals's GMP?
Current GMP certificates are on record from MHRA (UK) and ANVISA (Brazil). 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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Sources on this page

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