Suppliers / MEDA MANUFACTURING GmbH

MEDA MANUFACTURING GmbH

Germany 3 duplicate records merged Updated 9 July 2026

MEDA MANUFACTURING GmbH is a finished-dose manufacturer based in Germany. It appears in 13 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), INHRR (VE) and ARCSA (EC). Its GMP standing is certified by ANSM (FR), ZLG (DE) and EMA, among 5 authorities.

0
active US DMFs
0
valid CEPs
5
registered plants
13
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
Merignac, United Arab Emirates Not on file
COLOGNE (KÖLN), Germany Not on file
Cologne, Germany Not on file
Nordrhein-Westfalen, Germany Not on file
MERIGNAC, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 5 None
INHRR (VE) 4 None
ARCSA (EC) 4 None
ANSM (FR) None 7
ZLG (DE) None 4
EMA None 3
ANVISA (Brazil) None 1
EAEU_EEC None 1

Questions about MEDA MANUFACTURING GmbH

Does MEDA MANUFACTURING GmbH hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for MEDA MANUFACTURING GmbH. It does have 13 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does MEDA MANUFACTURING GmbH manufacture?
5 registered sites are on record, in United Arab Emirates, Germany and France (Merignac, Cologne (köln) and Cologne among others). Every site is listed on this page with the register it came from.
Which regulators recognise MEDA MANUFACTURING GmbH's GMP?
Current GMP certificates are on record from ANSM (FR), ZLG (DE), EMA, ANVISA (Brazil) and EEC (Eurasian Economic Union). 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