Suppliers / Eumedica Pharmaceuticals

Eumedica Pharmaceuticals

Belgium 205 employees Updated 9 July 2026

Eumedica Pharmaceuticals is a contract manufacturer based in Belgium. It appears in 98 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, ANSM (FR) and FAMHP (BE). Its GMP standing is certified by ZLG (DE) and EMA.

0
active US DMFs
0
valid CEPs
3
registered plants
98
filings across 10 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
Basel, Switzerland Not on file
Loerrach, Germany Not on file
Baden-Wuerttemberg, Germany Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 28 2
ANSM (FR) 15 None
FAMHP (BE) 13 None
AIFA (IT) 11 None
SWISSMEDIC (CH) 10 None
MPA (SE) 8 None
ZLG (DE) None 4

Questions about Eumedica Pharmaceuticals

Does Eumedica Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Eumedica Pharmaceuticals. It does have 98 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Eumedica Pharmaceuticals manufacture?
3 registered sites are on record, in Switzerland and Germany (Basel, Loerrach and Baden-wuerttemberg). Every site is listed on this page with the register it came from.
Which regulators recognise Eumedica Pharmaceuticals's GMP?
Current GMP certificates are on record from ZLG (DE) and 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.

Comparing suppliers?

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

Start for free
No sales call.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates