Suppliers / Bharat Serums and Vaccines

Bharat Serums and Vaccines

India 3 duplicate records merged Updated 9 July 2026

Bharat Serums and Vaccines is a finished-dose manufacturer based in India. It appears in 101 regulatory filings across 16 regulators, without an active US DMF or CEP on file. Its filings concentrate with TMDA (TZ), ZAMRA (ZM) and UZPHARM (UZ). Its GMP standing is certified by EMA, FDA (GH) and NAFDAC (NG), among 6 authorities. Customs aggregates show $80.1M of exports covering 1,531 molecules to 69 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
101
filings across 16 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
AMBARNATH, India Not on file
Thane, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
TMDA (TZ) 23 None
ZAMRA (ZM) 11 None
UZPHARM (UZ) 11 1
NAFDAC (NG) 11 1
CDSCO (India) 10 None
DIGEMAPS (DO) 8 None
EMA None 2
FDA (GH) None 1
EAEU_EEC None 1
ANVISA (Brazil) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $10.6M 38
2025 Not reported $80.1M 69
2024 Not reported $77.5M 74
2023 Not reported $82.6M 70

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 We do not publish the identity of any buyer.

Questions about Bharat Serums and Vaccines

Does Bharat Serums and Vaccines hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bharat Serums and Vaccines. It does have 101 filings with 16 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Bharat Serums and Vaccines manufacture?
2 registered sites are on record, in India (Ambarnath and Thane). Every site is listed on this page with the register it came from.
Which regulators recognise Bharat Serums and Vaccines's GMP?
Current GMP certificates are on record from EMA, FDA (GH), NAFDAC (NG), UZPHARM (UZ), EEC (Eurasian Economic Union) and 1 more. 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