Suppliers / Sai Mirra Innopharm

Sai Mirra Innopharm

India 27 employees Updated 9 July 2026

Sai Mirra Innopharm is a finished-dose manufacturer based in India. It appears in 33 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), NAFDAC (NG) and MINSA (CR). Its GMP standing is certified by CDSCO (India), FDA (GH) and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
4
registered plants
33
filings across 7 regulators

Registered plants

Site FDA FEI
AMBATTUR, India Not on file
chennai 98, India Not on file
Chennai, India Not on file
Chennai, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 11 None
NAFDAC (NG) 9 1
MINSA (CR) 4 None
ARCSA (EC) 3 None
FDA (GH) 3 1
DIGEMAPS (DO) 2 None
CDSCO (India) None 2

Questions about Sai Mirra Innopharm

Does Sai Mirra Innopharm hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sai Mirra Innopharm. It does have 33 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sai Mirra Innopharm manufacture?
4 registered sites are on record, in India and Nigeria (Ambattur, Chennai 98 and Chennai among others). Every site is listed on this page with the register it came from.
Which regulators recognise Sai Mirra Innopharm's GMP?
Current GMP certificates are on record from CDSCO (India), FDA (GH) and NAFDAC (NG). 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