Suppliers / UMEDICA Laboratories

UMEDICA Laboratories

India 618 employees 5 duplicate records merged Updated 9 July 2026

UMEDICA Laboratories is a finished-dose manufacturer based in India. It appears in 50 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), MINSA (CR) and ZAMRA (ZM). Its GMP standing is certified by CDSCO (India), EMA and FDA (GH), among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 29 March 2024 as VAI. Customs aggregates show $42.3M of exports covering 1,398 molecules to 92 destinations in 2025.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
50
filings across 11 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 29 March 2024 VAI US FDA
  • 5 July 2019 VAI US FDA
  • 19 January 2018 NAI US FDA
  • 9 October 2015 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Vapi, India 3008460260
Valsad, India Not on file
vadodara 390 019vadodara, India Not on file
vapivapi 396 195 valsad, India Not on file
changodarah medabad 382 213, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 15 None
MINSA (CR) 8 None
ZAMRA (ZM) 6 None
US FDA 5 1
TMDA (TZ) 4 None
BOMRA (BW) 3 None
CDSCO (India) None 4
EMA None 1
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $12.8M 70
2025 Not reported $42.3M 92
2024 Not reported $37.2M 44
2023 Not reported $21.6M 46

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 We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was VAI, on 29 March 2024.

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