Suppliers / Om Pharma

Om Pharma

Switzerland 597 employees Updated 9 July 2026

Om Pharma is a finished-dose manufacturer based in Switzerland. It appears in 59 regulatory filings across 13 regulators, without an active US DMF or CEP on file. Its filings concentrate with SWISSMEDIC (CH), INFARMED (PT) and EDE (AE). Its GMP standing is certified by EMA and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
5
registered plants
59
filings across 13 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
Meyrin 2/Geneva, United Arab Emirates Not on file
MEYRIN, Switzerland Not on file
Meyrin, Switzerland Not on file
AMADORA, Portugal Not on file
Amadora, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SWISSMEDIC (CH) 14 None
INFARMED (PT) 11 None
EDE (AE) 9 None
ARCSA (EC) 5 None
MINSA (CR) 5 None
SFDA (Saudi Arabia) 4 None
EMA None 4
ANVISA (Brazil) None 3

Questions about Om Pharma

Does Om Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Om Pharma. It does have 59 filings with 13 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Om Pharma manufacture?
5 registered sites are on record, in United Arab Emirates, Switzerland and Portugal (Meyrin 2/geneva, Meyrin and Meyrin among others). Every site is listed on this page with the register it came from.
Which regulators recognise Om Pharma's GMP?
Current GMP certificates are on record from EMA and ANVISA (Brazil). 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