Indofarma
Фармацевтические составы, дженерики и товары медицинского назначения.
Индофарма производит фармацевтические препараты, дженерики и товары медицинского назначения на своем предприятии в Бекаси. Компания поставляет продукцию аптекам, покупателям больниц, дистрибьюторам медицинских услуг или экспортным клиентам на перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Bekasi, Indonesia
- Founded
- 1918
- Website
- indofarma.id
- Categories
- Медицинские товары и расходники, БАДы и товары для здоровья
- Markets
- Индонезия, Сингапур, Малайзия, Филиппины
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)
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)