Suppliers / Mega Lifesciences Public

Mega Lifesciences Public

Thailand Updated 9 July 2026

Mega Lifesciences Public is a finished-dose manufacturer based in Thailand. It appears in 241 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), TMDA (TZ) and PPB (KE). Its GMP standing is certified by FDA (GH), EMA and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
4
registered plants
241
filings across 10 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Bangpoo Industrial Estate, United Arab Emirates Not on file
SAMUTPRAKAN, United Arab Emirates Not on file
Samutprakarn, United Arab Emirates Not on file
Mueang Samut Prakan, Thailand Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 104 None
TMDA (TZ) 54 None
PPB (KE) 44 None
UZPHARM (UZ) 11 None
MCAZ (ZW) 7 None
ZAMRA (ZM) 7 None
FDA (GH) None 1
EMA None 1
NAFDAC (NG) None 1

Questions about Mega Lifesciences Public

Does Mega Lifesciences Public hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mega Lifesciences Public. It does have 241 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Mega Lifesciences Public manufacture?
4 registered sites are on record, in United Arab Emirates and Thailand (Bangpoo Industrial Estate, Samutprakan and Samutprakarn among others). Every site is listed on this page with the register it came from.
Which regulators recognise Mega Lifesciences Public's GMP?
Current GMP certificates are on record from FDA (GH), EMA 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