Suppliers / Gulf Pharmaceutical Industries

Gulf Pharmaceutical Industries

United Arab Emirates Updated 9 July 2026

Gulf Pharmaceutical Industries is a finished-dose manufacturer based in United Arab Emirates. It appears in 793 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), SFDA (Saudi Arabia) and EFDA (ET). Its GMP standing is certified by TMDA (TZ) and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
793
filings across 8 regulators

Registered plants

Site FDA FEI
Ras Al Khaimah, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 447 None
SFDA (Saudi Arabia) 202 None
EFDA (ET) 64 None
ARCSA (EC) 41 None
JFDA (JO) 18 None
TMDA (TZ) 15 1
NAFDAC (NG) None 1

Questions about Gulf Pharmaceutical Industries

Does Gulf Pharmaceutical Industries hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Gulf Pharmaceutical Industries. It does have 793 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Gulf Pharmaceutical Industries manufacture?
1 registered site is on record, in United Arab Emirates (Ras Al Khaimah). Every site is listed on this page with the register it came from.
Which regulators recognise Gulf Pharmaceutical Industries's GMP?
Current GMP certificates are on record from TMDA (TZ) and NAFDAC (NG). 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