Kimia Farma
Kimia Farma производит дженерики для экспортных каналов B2B.
Kimia Farma производит дженерики, фармацевтические препараты и товары медицинского назначения в Джакарте. Основанная в 1817 году, компания снабжает аптеки, больницы, тендеры и регулируемых дистрибьюторов в ID, SG, MY, AU и на соответствующих экспортных рынках.
- Type
- brand seeking distribution
- Location
- Jakarta, Indonesia
- Founded
- 1817
- Website
- kimiafarma.co.id
- Categories
- Медицинские товары и расходники
- Markets
- Индонезия, Сингапур, Малайзия, Австралия
Verified facts
- product-authorised-for-sale (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of products authorised for sale in Indonesia (Cek Produk)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- certs-verified (green), checked 2026-08-19 Kemenkes e-Sertifikasi Alkes (Ministry of Health of Indonesia), medical-device certification lists
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
- domain-registered (green), checked 2026-08-08 Domain registry record
- registered-trade-role (green), checked 2026-08-19 Kemenkes e-Sertifikasi Alkes (Ministry of Health of Indonesia), medical-device certification lists
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)