Suppliers / Pt Simex Pharmaceutical Indonesia

Pt Simex Pharmaceutical Indonesia

Indonesia 325 employees Updated 9 July 2026

Pt Simex Pharmaceutical Indonesia is a finished-dose manufacturer based in Indonesia. It appears in 113 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
113
filings across 1 regulators

Registered plants

Site FDA FEI
KAB. SUKABUMI, Indonesia Not on file
-, Indonesia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 113 12

Questions about Pt Simex Pharmaceutical Indonesia

Does Pt Simex Pharmaceutical Indonesia hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pt Simex Pharmaceutical Indonesia. It does have 113 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pt Simex Pharmaceutical Indonesia manufacture?
2 registered sites are on record, in Indonesia (Kab. Sukabumi and -). Every site is listed on this page with the register it came from.
Which regulators recognise Pt Simex Pharmaceutical Indonesia'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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Sources on this page

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