Mega Lifesciences PCL
Fournisseur régional de bien-être distribuant des compléments nutritionnels et des actifs médicaux
Mega Lifesciences PCL exploite des chaînes de distribution hautement contrôlées pour les vitamines et les produits pharmaceutiques. L'entreprise travaille avec des installations de fabrication pour fournir des produits de santé sûrs dans les pays en développement. Leurs actifs logistiques répondent à des normes pharmaceutiques mondiales strictes.
- Type
- distributor seeking brands
- Location
- Bangkok, Thailand
- Founded
- 1982
- Website
- megawecare.com
- Categories
- Compléments et bien-être, Fournitures médicales et de santé
- Markets
- Thaïlande, Viêt Nam, Philippines
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- registry-activity (green), checked 2026-08-15 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- financials-published (green), checked 2025-12-31 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- registry-id-verified (green), checked 2026-08-20 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
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)