Suppliers / Synmedic Laboratories

Synmedic Laboratories

India 152 employees Updated 9 July 2026

Synmedic Laboratories is a finished-dose manufacturer based in India. It appears in 122 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), ARCSA (EC) and CDSCO (India). Its GMP standing is certified by EAEU_EEC.

0
active US DMFs
0
valid CEPs
0
registered plants
122
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
0 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 116 None
ARCSA (EC) 5 None
CDSCO (India) 1 None
EAEU_EEC None 2

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Synmedic Laboratories

Does Synmedic Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Synmedic Laboratories. It does have 122 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Synmedic Laboratories's GMP?
Current GMP certificates are on record from EEC (Eurasian Economic Union). 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates