Suppliers / Eris Lifesciences

Eris Lifesciences

India Updated 9 July 2026

Eris Lifesciences is a finished-dose manufacturer based in India. It appears in 31 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India).

0
active US DMFs
0
valid CEPs
2
registered plants
31
filings across 1 regulators

Registered plants

Site FDA FEI
guwahati 31 dist kamrup pin 781125 india, India Not on file
North, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 31 2

Questions about Eris Lifesciences

Does Eris Lifesciences hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Eris Lifesciences. It does have 31 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Eris Lifesciences manufacture?
2 registered sites are on record, in India (Guwahati 31 Dist Kamrup Pin 781125 India and North). Every site is listed on this page with the register it came from.
Which regulators recognise Eris Lifesciences's GMP?
Current GMP certificates are on record from CDSCO (India). 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