Suppliers / Pt Trifa Raya Laboratories

Pt Trifa Raya Laboratories

Indonesia Updated 9 July 2026

Pt Trifa Raya Laboratories is a finished-dose manufacturer based in Indonesia. It appears in 73 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by BPOM (ID).

0
active US DMFs
0
valid CEPs
2
registered plants
73
filings across 1 regulators

Registered plants

Site FDA FEI
KOTA BANDUNG, Indonesia Not on file
-, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 73 12

Questions about Pt Trifa Raya Laboratories

Does Pt Trifa Raya Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pt Trifa Raya Laboratories. It does have 73 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pt Trifa Raya Laboratories manufacture?
2 registered sites are on record, in Indonesia (Kota Bandung and -). Every site is listed on this page with the register it came from.
Which regulators recognise Pt Trifa Raya Laboratories's GMP?
Current GMP certificates are on record from BPOM (ID). 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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Comparable suppliers

Dankos Farma also in Indonesia Dexa Medica also in Indonesia Ferron Par Pharmaceuticals also in Indonesia Fonko International Pharmaceuticals also in Indonesia Medikon Prima Laboratories also in Indonesia

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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