Suppliers / M/s. Eris

M/s. Eris

India Updated 9 July 2026

M/s. Eris is a finished-dose manufacturer based in India. It appears in 59 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDA (EG), CDSCO (India) and DPM (TN).

0
active US DMFs
0
valid CEPs
0
registered plants
59
filings across 3 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 51 None
CDSCO (India) 6 None
DPM (TN) 2 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 M/s. Eris

Does M/s. Eris hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for M/s. Eris. It does have 59 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does M/s. Eris file?
Filings are on record with EDA (EG), CDSCO (India) and DPM (TN), 59 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