Suppliers / East Farm

East Farm

Uzbekistan Updated 9 July 2026

East Farm is a finished-dose manufacturer based in Uzbekistan. It appears in 407 regulatory filings across 20 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), AIFA (IT) and EMA. Its GMP standing is certified by UZPHARM (UZ), SAHPRA (ZA) and TMDA (TZ).

0
active US DMFs
0
valid CEPs
7
registered plants
407
filings across 20 regulators

Registered plants

Site FDA FEI
ATE, Peru Not on file
Arumeru, Tanzania Not on file
Samarkand Region, Uzbekistan Not on file
Syrdarya Region, Uzbekistan Not on file
Fergana Region, Uzbekistan Not on file
Fergana Region, Uzbekistan Not on file

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 146 6
AIFA (IT) 72 None
EMA 65 None
INHRR (VE) 35 None
INFARMED (PT) 17 None
Health Canada 15 None
SAHPRA (ZA) None 3
TMDA (TZ) None 3

Questions about East Farm

Does East Farm hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for East Farm. It does have 407 filings with 20 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does East Farm manufacture?
7 registered sites are on record, in Peru, Tanzania and Uzbekistan (ATE, Arumeru and Samarkand Region among others). Every site is listed on this page with the register it came from.
Which regulators recognise East Farm's GMP?
Current GMP certificates are on record from UZPHARM (UZ), SAHPRA (ZA) 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.

Comparing suppliers?

Choose your molecules and target markets. East Farm comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

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