Suppliers / Tty Biopharm

Tty Biopharm

Taiwan 241 employees Updated 9 July 2026

Tty Biopharm is a finished-dose manufacturer based in Taiwan. It appears in 19 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), NPRA (MY) and INVIMA (CO). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
19
filings across 4 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
Chung-Li, Taiwan Not on file
Keelung City, Taiwan Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 14 None
NPRA (MY) 3 None
INVIMA (CO) 1 None
JFDA (JO) 1 None
EMA None 3

Questions about Tty Biopharm

Does Tty Biopharm hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Tty Biopharm. It does have 19 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Tty Biopharm manufacture?
2 registered sites are on record, in Taiwan (Chung-li and Keelung City). Every site is listed on this page with the register it came from.
Which regulators recognise Tty Biopharm's GMP?
Current GMP certificates are on record from EMA. 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