Suppliers / Medochemie

Medochemie

Cyprus 895 employees 3 duplicate records merged Updated 9 July 2026

Medochemie is a finished-dose manufacturer based in Cyprus. It appears in 681 regulatory filings across 20 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, DAV (Vietnam) and EFDA (ET). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
4
registered plants
681
filings across 20 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
Agios Athanassios, United Arab Emirates Not on file
Limassol, United Arab Emirates Not on file
Agios Athanasios, Cyprus Not on file
Limassol, Cyprus Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 250 2
DAV (Vietnam) 159 None
EFDA (ET) 64 None
INFARMED (PT) 53 None
MPA (SE) 37 None
SFDA (Saudi Arabia) 28 None

Questions about Medochemie

Does Medochemie hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Medochemie. It does have 681 filings with 20 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Medochemie manufacture?
4 registered sites are on record, in United Arab Emirates and Cyprus (Agios Athanassios, Limassol and Agios Athanasios among others). Every site is listed on this page with the register it came from.
Which regulators recognise Medochemie's GMP?
Current GMP certificates are on record from EMA. 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