Suppliers / Gensenta Ilaç Sanayi Ve Ticaret

Gensenta Ilaç Sanayi Ve Ticaret

Turkey Updated 9 July 2026

Gensenta Ilaç Sanayi Ve Ticaret is a finished-dose manufacturer based in Turkey. It appears in 8 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANPP (DZ), MINSA (CR) and DIGEMAPS (DO). Its GMP standing is certified by EMA and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
3
registered plants
8
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
Istanbul, United Arab Emirates Not on file
ISTAMBUL, Turkey Not on file
Bahcelievler, Turkey Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANPP (DZ) 3 None
MINSA (CR) 2 None
DIGEMAPS (DO) 2 None
INVIMA (CO) 1 None
EMA None 4
ANVISA (Brazil) None 1

Questions about Gensenta Ilaç Sanayi Ve Ticaret

Does Gensenta Ilaç Sanayi Ve Ticaret hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Gensenta Ilaç Sanayi Ve Ticaret. It does have 8 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Gensenta Ilaç Sanayi Ve Ticaret manufacture?
3 registered sites are on record, in United Arab Emirates and Turkey (Istanbul, Istambul and Bahcelievler). Every site is listed on this page with the register it came from.
Which regulators recognise Gensenta Ilaç Sanayi Ve Ticaret's GMP?
Current GMP certificates are on record from EMA and ANVISA (Brazil). 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