Suppliers / Pt. Tempo Scan Pacific Tbk

Pt. Tempo Scan Pacific Tbk

Indonesia Updated 9 July 2026

Pt. Tempo Scan Pacific Tbk is a finished-dose manufacturer based in Indonesia. It appears in 173 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with BPOM (ID) and NAFDAC (NG). Its GMP standing is certified by BPOM (ID) and NAFDAC (NG). Customs aggregates show $13.2M of exports covering 39 molecules to 2 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
173
filings across 2 regulators

Registered plants

Site FDA FEI
-, Indonesia Not on file
KAB. BEKASI, Indonesia Not on file
Cikarang Bekassi Indonesia, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BPOM (ID) 169 14
NAFDAC (NG) 4 3

Scale

Year Revenue Exports Destinations
2025 Not reported $13.2M 2
2024 Not reported $15.6M 3

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Pt. Tempo Scan Pacific Tbk

Does Pt. Tempo Scan Pacific Tbk hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pt. Tempo Scan Pacific Tbk. It does have 173 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pt. Tempo Scan Pacific Tbk manufacture?
3 registered sites are on record, in Indonesia and Nigeria (-, Kab. Bekasi and Cikarang Bekassi Indonesia). Every site is listed on this page with the register it came from.
Which regulators recognise Pt. Tempo Scan Pacific Tbk's GMP?
Current GMP certificates are on record from BPOM (ID) 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.

Comparing suppliers?

Choose your molecules and target markets. Pt. Tempo Scan Pacific Tbk comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts