Suppliers / Humanis Saglik A S

Humanis Saglik A S

Turkey Updated 9 July 2026

Humanis Saglik A S is a finished-dose manufacturer based in Turkey. It appears in 225 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with TITCK (TR), EFDA (ET) and RAMA (GE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
225
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
Kapakli, Turkey Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
TITCK (TR) 198 None
EFDA (ET) 13 None
RAMA (GE) 6 None
TMDA (TZ) 5 None
UZPHARM (UZ) 3 None
EMA None 1

Comparing suppliers?

Choose your molecules and target markets. Humanis Saglik A S comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

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