Suppliers / Esteve Pharmaceuticals

Esteve Pharmaceuticals

Spain Updated 9 July 2026

Esteve Pharmaceuticals is a finished-dose manufacturer based in Spain. It appears in 487 regulatory filings across 12 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, MHRA (UK) and AEMPS (ES). Its GMP standing is certified by MHRA (UK).

0
active US DMFs
0
valid CEPs
1
registered plants
487
filings across 12 regulators

Registered plants

Site FDA FEI
MAIDENHEAD, United Kingdom Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 205 None
MHRA (UK) 103 1
AEMPS (ES) 87 None
AIFA (IT) 19 None
DMP (NO) 17 None
MPA (SE) 15 None

Questions about Esteve Pharmaceuticals

Does Esteve Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Esteve Pharmaceuticals. It does have 487 filings with 12 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Esteve Pharmaceuticals manufacture?
1 registered site is on record, in United Kingdom (Maidenhead). Every site is listed on this page with the register it came from.
Which regulators recognise Esteve Pharmaceuticals'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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Sources on this page

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