Mega Lifesciences PCL
Региональный поставщик оздоровительных услуг, распространяющий пищевые добавки и медицинские товары
Mega Lifesciences PCL управляет строго контролируемыми цепочками сбыта витаминов и фармацевтических препаратов. Компания сотрудничает с производственными предприятиями, чтобы поставлять безопасную медицинскую продукцию в развивающиеся страны. Их логистические активы соответствуют строгим мировым фармацевтическим стандартам.
- Type
- distributor seeking brands
- Location
- Bangkok, Thailand
- Founded
- 1982
- Website
- megawecare.com
- Categories
- БАДы и товары для здоровья, Медицинские товары и расходники
- Markets
- Таиланд, Вьетнам, Филиппины
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)