Suppliers / Rowa Pharmaceuticals

Rowa Pharmaceuticals

Ireland Updated 9 July 2026

Rowa Pharmaceuticals is a finished-dose manufacturer based in Ireland. It appears in 80 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, ARCSA (EC) and UZPHARM (UZ). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
80
filings across 3 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
Bantry Co Cork, United Arab Emirates Not on file
Co. Cork, Ireland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 75 1
ARCSA (EC) 3 None
UZPHARM (UZ) 2 None

Questions about Rowa Pharmaceuticals

Does Rowa Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Rowa Pharmaceuticals. It does have 80 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Rowa Pharmaceuticals manufacture?
2 registered sites are on record, in United Arab Emirates and Ireland (Bantry Co Cork and Co. Cork). Every site is listed on this page with the register it came from.
Which regulators recognise Rowa Pharmaceuticals'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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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