Suppliers / MultiPharma

MultiPharma

20 employees Updated 9 July 2026

MultiPharma is a finished-dose manufacturer. It appears in 104 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with INHRR (VE), ARCSA (EC) and EDA (EG).

0
active US DMFs
0
valid CEPs
0
registered plants
104
filings across 3 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
INHRR (VE) 57 None
ARCSA (EC) 30 None
EDA (EG) 17 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about MultiPharma

Does MultiPharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for MultiPharma. It does have 104 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does MultiPharma file?
Filings are on record with INHRR (VE), ARCSA (EC) and EDA (EG), 104 in total.

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