Mega Lifesciences PCL
栄養補助食品や医療資産を販売する地域のウェルネス サプライヤー
Mega Lifesciences PCL は、ビタミンと医薬品の高度に管理された流通チェーンを運営しています。同社は製造施設と協力して、発展途上国全体に安全なヘルスケア製品を提供しています。同社の物流資産は厳格な世界的な医薬品基準を満たしています。
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Bangkok, Thailand
- Founded
- 1982
- Website
- megawecare.com
- Categories
- サプリメントとウェルネス, 医療およびヘルスケア用品
- Markets
- タイ, ベトナム, フィリピン
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
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), effective since 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, not confirmed by us
- 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)