Suppliers / GEBRO PHARMA

GEBRO PHARMA

Austria 65 employees Updated 9 July 2026

GEBRO PHARMA is a finished-dose manufacturer based in Austria. It appears in 182 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with SWISSMEDIC (CH), EMA and MPA (SE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
4
registered plants
182
filings across 9 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
FIEBERBRUNN, Austria Not on file
Tyrol, Austria Not on file
Liestal, Switzerland Not on file
Lausen, Switzerland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SWISSMEDIC (CH) 85 None
EMA 79 2
MPA (SE) 4 None
DMP (NO) 3 None
INFARMED (PT) 3 None
MINSA (CR) 3 None

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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