Suppliers / Elpen Pharmaceutical

Elpen Pharmaceutical

Greece Updated 9 July 2026

Elpen Pharmaceutical is a finished-dose manufacturer based in Greece. It appears in 115 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with MPA (SE), AIFA (IT) and ARCSA (EC).

0
active US DMFs
0
valid CEPs
2
registered plants
115
filings across 10 regulators

Registered plants

Site FDA FEI
Attica, United Arab Emirates Not on file
Keratea, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MPA (SE) 45 None
AIFA (IT) 23 None
ARCSA (EC) 9 None
INFARMED (PT) 9 None
EMA 8 None
AEMPS (ES) 8 None

Questions about Elpen Pharmaceutical

Does Elpen Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Elpen Pharmaceutical. It does have 115 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Elpen Pharmaceutical manufacture?
2 registered sites are on record, in United Arab Emirates (Attica and Keratea). Every site is listed on this page with the register it came from.
Where does Elpen Pharmaceutical file?
Filings are on record with MPA (SE), AIFA (IT), ARCSA (EC), INFARMED (PT) and 6 other regulators, 115 in total.

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