Suppliers / Sanovel Ilac Sanayi Ve Ticaret A S

Sanovel Ilac Sanayi Ve Ticaret A S

Turkey 2 duplicate records merged Updated 9 July 2026

Sanovel Ilac Sanayi Ve Ticaret A S is a finished-dose manufacturer based in Turkey. It appears in 42 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with RAMA (GE), UZPHARM (UZ) and ARCSA (EC). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
42
filings across 3 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
Silivri, Turkey Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
RAMA (GE) 19 None
UZPHARM (UZ) 19 None
ARCSA (EC) 4 None
EMA None 1

Questions about Sanovel Ilac Sanayi Ve Ticaret A S

Does Sanovel 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 Sanovel Ilac Sanayi Ve Ticaret A S. It does have 42 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sanovel Ilac Sanayi Ve Ticaret A S manufacture?
1 registered site is on record, in Turkey (Silivri). Every site is listed on this page with the register it came from.
Which regulators recognise Sanovel 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.

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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