Suppliers / Globela Pharma

Globela Pharma

India 68 employees 3 duplicate records merged Updated 9 July 2026

Globela Pharma is a finished-dose manufacturer based in India. It appears in 188 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), ARCSA (EC) and DIGEMAPS (DO). Its GMP standing is certified by CDSCO (India) and EMA. Customs aggregates show $28.6M of exports covering 1,331 molecules to 45 destinations in 2025.

0
active US DMFs
0
valid CEPs
6
registered plants
188
filings across 8 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
sachin surat 394 230, India Not on file
G.I.D.C., India Not on file
Surat, India Not on file
G.I.D.C., India Not on file
tal umbergaonvalsad 396 105, India Not on file
valsad, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 139 None
ARCSA (EC) 30 None
DIGEMAPS (DO) 11 None
EFDA (ET) 3 None
BOMRA (BW) 2 None
MINSA (CR) 1 None
CDSCO (India) None 6
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3K 1
2025 Not reported $28.6M 45
2024 Not reported $23.0M 45
2023 Not reported $20.1M 37

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 We do not publish the identity of any buyer.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