Suppliers / Chemo India Formulation

Chemo India Formulation

India 110 employees Updated 9 July 2026

Chemo India Formulation is a finished-dose manufacturer based in India. It appears in 9 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), INVIMA (CO) and DIGEMAPS (DO). Its GMP standing is certified by EMA. Customs aggregates show $3.7M of exports covering 665 molecules to 13 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
9
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
Hyderabad, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 3 None
INVIMA (CO) 3 None
DIGEMAPS (DO) 3 None
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.4M 7
2025 Not reported $3.7M 13
2024 Not reported $1.8M 8
2023 Not reported $2.5M 5

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 We do not publish the identity of any buyer.

Questions about Chemo India Formulation

Does Chemo India Formulation hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Chemo India Formulation. It does have 9 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Chemo India Formulation manufacture?
1 registered site is on record, in India (Hyderabad). Every site is listed on this page with the register it came from.
Which regulators recognise Chemo India Formulation's GMP?
Current GMP certificates are on record from EMA. 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
Customs aggregates
Export values, molecule and destination counts