Suppliers / Saja Pharmaceuticals

Saja Pharmaceuticals

Saudi Arabia Updated 9 July 2026

Saja Pharmaceuticals is a finished-dose manufacturer based in Saudi Arabia. It appears in 61 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDA (EG), EDE (AE) and JFDA (JO). Its GMP standing is certified by EDA (EG).

0
active US DMFs
0
valid CEPs
1
registered plants
61
filings across 3 regulators

Registered plants

Site FDA FEI
6th of October City, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 36 1
EDE (AE) 24 None
JFDA (JO) 1 None

Questions about Saja Pharmaceuticals

Does Saja Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Saja Pharmaceuticals. It does have 61 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Saja Pharmaceuticals manufacture?
1 registered site is on record, in United Arab Emirates (6th Of October City). Every site is listed on this page with the register it came from.
Which regulators recognise Saja Pharmaceuticals's GMP?
Current GMP certificates are on record from EDA (EG). 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