Suppliers / Dawa

Dawa

Kenya 16 employees 2 duplicate records merged Updated 9 July 2026

Dawa is a finished-dose manufacturer based in Kenya. It appears in 855 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with PPB (KE), EMA and EDA (EG). Its GMP standing is certified by PPB (KE) and TMDA (TZ).

0
active US DMFs
0
valid CEPs
2
registered plants
855
filings across 7 regulators

Registered plants

Site FDA FEI
Nairobi, Kenya Not on file
Damad, Saudi Arabia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
PPB (KE) 662 1
EMA 85 None
EDA (EG) 49 None
ZAMRA (ZM) 47 None
TMDA (TZ) 9 1
MHRA (UK) 2 None

Questions about Dawa

Does Dawa hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dawa. It does have 855 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Dawa manufacture?
2 registered sites are on record, in Kenya and Saudi Arabia (Nairobi and Damad). Every site is listed on this page with the register it came from.
Which regulators recognise Dawa's GMP?
Current GMP certificates are on record from PPB (KE) 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.

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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