Suppliers / Orion

Orion

Finland 512 employees 4 duplicate records merged Updated 9 July 2026

Orion is a finished-dose manufacturer based in Finland. It appears in 2,474 regulatory filings across 27 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, MPA (SE) and DKMA (DK). Its GMP standing is certified by MFDS (Korea), ANVISA (Brazil) and NCELS (KZ), among 6 authorities.

0
active US DMFs
0
valid CEPs
5
registered plants
2,474
filings across 27 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
Espoo, United Arab Emirates Not on file
Salo, United Arab Emirates Not on file
Zug, Switzerland Not on file
SALO, Finland Not on file
Fermion Espoo, Finland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 712 1
MPA (SE) 628 None
DKMA (DK) 291 None
AIFA (IT) 181 None
FAMHP (BE) 152 None
DMP (NO) 95 None
MFDS (Korea) None 4
ANVISA (Brazil) None 4
NCELS (KZ) None 3
EAEU_EEC None 2
HSA (SG) None 2

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Open risk flags

  • 1 active litigation matter is on record.

Sources on this page

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