Suppliers / Proventus Life Sciences

Proventus Life Sciences

India 61 employees 2 duplicate records merged Updated 9 July 2026

Proventus Life Sciences is an API manufacturer based in India. It holds one valid CEP. Its GMP standing is certified by CDSCO (India). Customs aggregates show $399K of exports covering 8 molecules to 7 destinations in 2025.

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

Registered plants

Site FDA FEI
Chengalpattu District, India Not on file
Kancheepuram, India Not on file

What they file, and where

Molecule Regulators Docs
Primidone EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $572K 1
2025 Not reported $399K 7

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 We do not publish the identity of any buyer.

Questions about Proventus Life Sciences

Does Proventus Life Sciences hold a US DMF or a CEP?
Proventus Life Sciences holds 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Proventus Life Sciences manufacture?
2 registered sites are on record, in India (Chengalpattu District and Kancheepuram). Every site is listed on this page with the register it came from.
What does Proventus Life Sciences make?
1 molecule is on record against Proventus Life Sciences, including Primidone. Each links through to that molecule's full manufacturer list.
Which regulators recognise Proventus Life Sciences'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
Customs aggregates
Export values, molecule and destination counts