Suppliers / Mefar İlaç Sanayii A.Ş

Mefar İlaç Sanayii A.Ş

Turkey Updated 9 July 2026

Mefar İlaç Sanayii A.Ş is a finished-dose manufacturer based in Turkey. It appears in 36 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), NPRA (MY) and INVIMA (CO). Its GMP standing is certified by EMA and EAEU_EEC.

0
active US DMFs
0
valid CEPs
2
registered plants
36
filings across 5 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
Istanbul, United Arab Emirates Not on file
Pendik, Turkey Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 30 None
NPRA (MY) 3 None
INVIMA (CO) 1 None
EDE (AE) 1 None
MINSA (CR) 1 None
EMA None 8
EAEU_EEC None 2

Questions about Mefar İlaç Sanayii A.Ş

Does Mefar İlaç Sanayii A.Ş hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mefar İlaç Sanayii A.Ş. It does have 36 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Mefar İlaç Sanayii A.Ş manufacture?
2 registered sites are on record, in United Arab Emirates and Turkey (Istanbul and Pendik). Every site is listed on this page with the register it came from.
Which regulators recognise Mefar İlaç Sanayii A.Ş's GMP?
Current GMP certificates are on record from EMA and 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