Suppliers / Unison Laboratories

Unison Laboratories

Thailand Updated 9 July 2026

Unison Laboratories is a finished-dose manufacturer based in Thailand. It appears in 131 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with NPRA (MY), DAV (Vietnam) and JFDA (JO). Its GMP standing is certified by HSA (SG).

0
active US DMFs
0
valid CEPs
1
registered plants
131
filings across 4 regulators

Registered plants

Site FDA FEI
Chachoengsao, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NPRA (MY) 106 None
DAV (Vietnam) 20 None
JFDA (JO) 4 None
EDE (AE) 1 None
HSA (SG) None 1

Questions about Unison Laboratories

Does Unison Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Unison Laboratories. It does have 131 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Unison Laboratories manufacture?
1 registered site is on record, in United Arab Emirates (Chachoengsao). Every site is listed on this page with the register it came from.
Which regulators recognise Unison Laboratories's GMP?
Current GMP certificates are on record from HSA (SG). 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