Suppliers / Anabiosis

Anabiosis

India Updated 9 July 2026

Anabiosis is a finished-dose manufacturer based in India. It appears in 33 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, MPA (SE) and INFARMED (PT). Its GMP standing is certified by CDSCO (India) and FDA (GH).

0
active US DMFs
0
valid CEPs
1
registered plants
33
filings across 3 regulators

Registered plants

Site FDA FEI
dehgamgandhinaga r 382 305, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 19 None
MPA (SE) 8 None
INFARMED (PT) 6 None
CDSCO (India) None 2
FDA (GH) None 1

Questions about Anabiosis

Does Anabiosis hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Anabiosis. It does have 33 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Anabiosis manufacture?
1 registered site is on record, in India (Dehgamgandhinaga R 382 305). Every site is listed on this page with the register it came from.
Which regulators recognise Anabiosis's GMP?
Current GMP certificates are on record from CDSCO (India) and FDA (GH). 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