Suppliers / Vem Ilac Sanayi Ve Ticaret A S

Vem Ilac Sanayi Ve Ticaret A S

Turkey Updated 9 July 2026

Vem Ilac Sanayi Ve Ticaret A S is a contract manufacturer based in Turkey. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
1
filings across 1 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
ARCSA (EC) 1 None
EMA None 1

Questions about Vem Ilac Sanayi Ve Ticaret A S

Does Vem Ilac Sanayi Ve Ticaret A S hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Vem Ilac Sanayi Ve Ticaret A S. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Vem Ilac Sanayi Ve Ticaret A S manufacture?
1 registered site is on record, in Turkey (Kapakli). Every site is listed on this page with the register it came from.
Which regulators recognise Vem Ilac Sanayi Ve Ticaret A S'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.

Comparing suppliers?

Choose your molecules and target markets. Vem Ilac Sanayi Ve Ticaret A S comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Abdi Ibrahim Ilac Sanayi Ve Ticaret also in Turkey Atabay Ki̇mya Sanayi̇ Ti̇caret A.Ş also in Turkey Berko Ilac Ve Kimya Sanayi also in Turkey Bilim Ilac Sanayi Ve Ticaret A S also in Turkey Biofarma also in Turkey

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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