Suppliers / Anfarm Hellas

Anfarm Hellas

Greece Updated 9 July 2026

Anfarm Hellas is a finished-dose manufacturer based in Greece. It appears in 31 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EFDA (ET) and BOMRA (BW). Its GMP standing is certified by EAEU_EEC.

0
active US DMFs
0
valid CEPs
2
registered plants
31
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Schimatari- Viotias, United Arab Emirates Not on file
Sximatari- Viotia, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 16 None
EFDA (ET) 11 None
BOMRA (BW) 2 None
SFDA (Saudi Arabia) 2 None
EAEU_EEC None 1

Questions about Anfarm Hellas

Does Anfarm Hellas hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Anfarm Hellas. 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 Anfarm Hellas manufacture?
2 registered sites are on record, in United Arab Emirates (Schimatari- Viotias and Sximatari- Viotia). Every site is listed on this page with the register it came from.
Which regulators recognise Anfarm Hellas's GMP?
Current GMP certificates are on record from EEC (Eurasian Economic Union). 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