Suppliers / Saudi Pharmaceutical Industries And Medical Appliances

Saudi Pharmaceutical Industries And Medical Appliances

Saudi Arabia Updated 9 July 2026

Saudi Pharmaceutical Industries And Medical Appliances is a finished-dose manufacturer based in Saudi Arabia. It appears in 155 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), SFDA (Saudi Arabia) and JFDA (JO). Its GMP standing is certified by UZPHARM (UZ) and TMDA (TZ).

0
active US DMFs
0
valid CEPs
2
registered plants
155
filings across 7 regulators

Registered plants

Site FDA FEI
Al-Qassim, United Arab Emirates Not on file
Al-Qassim, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 107 None
SFDA (Saudi Arabia) 35 None
JFDA (JO) 5 None
FDA (GH) 3 None
ANPP (DZ) 3 None
UZPHARM (UZ) 1 2
TMDA (TZ) None 1

Questions about Saudi Pharmaceutical Industries And Medical Appliances

Does Saudi Pharmaceutical Industries And Medical Appliances hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Saudi Pharmaceutical Industries And Medical Appliances. It does have 155 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Saudi Pharmaceutical Industries And Medical Appliances manufacture?
2 registered sites are on record, in United Arab Emirates (Al-qassim among others). Every site is listed on this page with the register it came from.
Which regulators recognise Saudi Pharmaceutical Industries And Medical Appliances's GMP?
Current GMP certificates are on record from UZPHARM (UZ) 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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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