Suppliers / Deva Holding

Deva Holding

Turkey Updated 9 July 2026

Deva Holding is an API and finished-dose manufacturer based in Turkey. It holds 6 active US drug master files across a filed portfolio of 7 molecules. Its filings concentrate with RAMA (GE), UZPHARM (UZ) and EFDA (ET). Its GMP standing is certified by EMA, EAEU_EEC and TMDA (TZ).

6
active US DMFs
0
valid CEPs
4
registered plants
143
filings across 12 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
Tekirdag, United Arab Emirates Not on file
Kocaeli, United Arab Emirates Not on file
Kartepe, Turkey Not on file
Kapakli, Turkey Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
RAMA (GE) 52 None
UZPHARM (UZ) 35 None
EFDA (ET) 27 None
MINSA (CR) 9 None
DIGEMAPS (DO) 7 None
US FDA 6 None
EMA None 6
EAEU_EEC None 1
TMDA (TZ) None 1

Questions about Deva Holding

Does Deva Holding hold a US DMF or a CEP?
Deva Holding holds 6 active US drug master files. 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 Holding manufacture?
4 registered sites are on record, in United Arab Emirates and Turkey (Tekirdag, Kocaeli and Kartepe among others). Every site is listed on this page with the register it came from.
What does Deva Holding make?
7 molecules are on record against Deva Holding, including Amlodipine Mesilate, Dasatinib, Eltrombopag and Isoprenaline. Each links through to that molecule's full manufacturer list.
Which regulators recognise Deva Holding's GMP?
Current GMP certificates are on record from EMA, EEC (Eurasian Economic Union) and TMDA (TZ). 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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Open risk flags

  • 1 active litigation matter is on record.

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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