Suppliers / Cubit Lifesciences

Cubit Lifesciences

India 88 employees Updated 9 July 2026

Cubit Lifesciences is a finished-dose manufacturer based in India. It appears in 21 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), BOMRA (BW) and MINSA (CR). Its GMP standing is certified by CDSCO (India), FDA (GH) and TMDA (TZ), among 5 authorities. Customs aggregates show $878K of exports covering 119 molecules to 11 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
21
filings across 3 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
Bhayla, India Not on file
tal bavlaahmedabad 382 220, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 14 None
BOMRA (BW) 5 None
MINSA (CR) 2 None
CDSCO (India) None 2
FDA (GH) None 1
TMDA (TZ) None 1
EMA None 1
MCAZ (ZW) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $200K 5
2025 Not reported $878K 11
2024 Not reported $408K 5
2023 Not reported $408K 2

Export figures are customs aggregates. We do not publish the identity of any buyer.

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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
Customs aggregates
Export values, molecule and destination counts