Suppliers / DEVA HOLDİNG A.Ş. (2020/3) (Hammadde)

DEVA HOLDİNG A.Ş. (2020/3) (Hammadde)

Turkey Updated 9 July 2026

DEVA HOLDİNG A.Ş. (2020/3) (Hammadde) is an API and finished-dose manufacturer based in Turkey. It holds 4 valid CEPs across a filed portfolio of 4 molecules. Its filings concentrate with TITCK (TR), NCELS (KZ) and MCAZ (ZW).

0
active US DMFs
4
valid CEPs
1
registered plants
579
filings across 3 regulators

Registered plants

Site FDA FEI
Istanbul, Turkey Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
TITCK (TR) 570 None
NCELS (KZ) 8 None
MCAZ (ZW) 1 None

Questions about DEVA HOLDİNG A.Ş. (2020/3) (Hammadde)

Does DEVA HOLDİNG A.Ş. (2020/3) (Hammadde) hold a US DMF or a CEP?
DEVA HOLDİNG A.Ş. (2020/3) (Hammadde) holds 4 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does DEVA HOLDİNG A.Ş. (2020/3) (Hammadde) manufacture?
1 registered site is on record, in Turkey (Istanbul). Every site is listed on this page with the register it came from.
What does DEVA HOLDİNG A.Ş. (2020/3) (Hammadde) make?
4 molecules are on record against DEVA HOLDİNG A.Ş. (2020/3) (Hammadde), including Benserazide, Fingolimod, Imatinib Mesilate and Tiotropium. Each links through to that molecule's full manufacturer list.
Where does DEVA HOLDİNG A.Ş. (2020/3) (Hammadde) file?
Filings are on record with TITCK (TR), NCELS (KZ) and MCAZ (ZW), 579 in total.

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