Suppliers / PharmEvo

PharmEvo

Pakistan 2 duplicate records merged Updated 9 July 2026

PharmEvo is a finished-dose manufacturer based in Pakistan. It appears in 50 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), NAFDAC (NG) and EEC_EAEU. Its GMP standing is certified by NAFDAC (NG), UZPHARM (UZ) and DRAP (PK), among 4 authorities.

0
active US DMFs
0
valid CEPs
2
registered plants
50
filings across 5 regulators

Registered plants

Site FDA FEI
Karachi, Nigeria Not on file
karachi, Pakistan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 24 None
NAFDAC (NG) 14 3
EEC_EAEU 4 None
BOMRA (BW) 4 None
UZPHARM (UZ) 4 2
DRAP (PK) None 1
FDA (GH) None 1

Questions about PharmEvo

Does PharmEvo hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for PharmEvo. It does have 50 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does PharmEvo manufacture?
2 registered sites are on record, in Nigeria and Pakistan (Karachi and Karachi). Every site is listed on this page with the register it came from.
Which regulators recognise PharmEvo's GMP?
Current GMP certificates are on record from NAFDAC (NG), UZPHARM (UZ), DRAP (PK) and FDA (GH). 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