Suppliers / Aristo Pharma

Aristo Pharma

Germany 125 employees Updated 9 July 2026

Aristo Pharma is a finished-dose manufacturer based in Germany. It appears in 1,448 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with AEMPS (ES), AIFA (IT) and INFARMED (PT). Its GMP standing is certified by ZLG (DE) and EMA.

0
active US DMFs
0
valid CEPs
3
registered plants
1,448
filings across 11 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
Berlin, Germany Not on file
Alcochete, Portugal Not on file
Alcochete, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) 503 None
AIFA (IT) 375 None
INFARMED (PT) 260 None
MPA (SE) 149 None
MHRA (UK) 116 None
DMP (NO) 16 None
ZLG (DE) None 6
EMA None 1

Questions about Aristo Pharma

Does Aristo Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Aristo Pharma. It does have 1,448 filings with 11 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Aristo Pharma manufacture?
3 registered sites are on record, in Germany and Portugal (Berlin and Alcochete among others). Every site is listed on this page with the register it came from.
Which regulators recognise Aristo Pharma'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.

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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