Suppliers / Bimeda AMEA

Bimeda AMEA

Kenya 8 employees Updated 9 July 2026

Bimeda AMEA is a finished-dose manufacturer based in Kenya. It appears in 137 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with PPB (KE), TMDA (TZ) and ZAMRA (ZM). Its GMP standing is certified by TMDA (TZ).

0
active US DMFs
0
valid CEPs
0
registered plants
137
filings across 5 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
PPB (KE) 65 None
TMDA (TZ) 35 1
ZAMRA (ZM) 23 None
DKMA (DK) 12 None
MCAZ (ZW) 2 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Bimeda AMEA

Does Bimeda AMEA hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bimeda AMEA. It does have 137 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Bimeda AMEA's GMP?
Current GMP certificates are on record from 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