PT Kalbe Farma Tbk
La più grande azienda farmaceutica e di integratori sanitari quotata in borsa del Sud-Est asiatico.
PT Kalbe Farma Tbk è la più grande azienda farmaceutica e sanitaria di consumo quotata in borsa dell'Indonesia e del Sud-est asiatico, che produce farmaci da prescrizione, medicinali da banco, integratori alimentari e prodotti sanitari funzionali con marchi tra cui Extra Joss, Fitbar, Diabetasol e Prenagen. Kalbe International gestisce le esportazioni e il commercio transfrontaliero del gruppo nel sud-est asiatico e in Africa, con strutture stabilite in Nigeria per servire i mercati africani. L'azienda collabora attivamente con distributori all'ingrosso per le sue linee di integratori alimentari e per la salute dei consumatori in tutta l'ASEAN e oltre.
- Type
- brand seeking distribution
- Location
- Jakarta, Indonesia
- Founded
- 1966
- Website
- kalbe.co.id
- Categories
- Integratori e benessere, Forniture medicali e sanitarie
- Markets
- Malaysia, Singapore, Vietnam, Thailandia, Filippine, Nigeria, Sudafrica
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
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-08 Domain registry record
- 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)