Suppliers / Global Advanced pharmaceuticals "GAP"

Global Advanced pharmaceuticals "GAP"

Egypt Updated 9 July 2026

Global Advanced pharmaceuticals "GAP" is a finished-dose manufacturer based in Egypt. It appears in 38 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
38
filings across 1 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
Giza, Egypt Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 38 None
EMA None 1

Questions about Global Advanced pharmaceuticals "GAP"

Does Global Advanced pharmaceuticals "GAP" hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Global Advanced pharmaceuticals "GAP". It does have 38 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Global Advanced pharmaceuticals "GAP" manufacture?
1 registered site is on record, in Egypt (Giza). Every site is listed on this page with the register it came from.
Which regulators recognise Global Advanced pharmaceuticals "GAP"'s GMP?
Current GMP certificates are on record from EMA. 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