Suppliers / Sterinova

Sterinova

Canada Updated 9 July 2026

Sterinova is a finished-dose manufacturer based in Canada. It appears in 5 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada and US FDA.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
5
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Canada, Canada 3011699563

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 4 None
US FDA 1 None

Questions about Sterinova

Does Sterinova hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sterinova. It does have 5 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Sterinova FDA-registered?
One site operated by Sterinova carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Sterinova manufacture?
1 registered site is on record, in Canada (Canada). Every site is listed on this page with the register it came from.
Where does Sterinova file?
Filings are on record with Health Canada and US FDA, 5 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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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