Apex Healthcare Berhad
Red regional de distribución de atención sanitaria que gestiona productos farmacéuticos y de salud de consumo.
Apex Healthcare Berhad suministra medicamentos genéricos, herramientas de diagnóstico y artículos de atención quirúrgica. Sus centros de distribución ofrecen una cobertura completa de almacenamiento en frío para farmacias regionales. Garantizan una entrega diaria fluida de productos en todos los territorios del sudeste asiático.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Melaka, Malaysia
- Founded
- 1962
- Website
- apexhealthcare.com.my
- Categories
- Suministros médicos y sanitarios, Cuidado personal
- Markets
- Malasia, Singapur
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 2026-08-04 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- Good Manufacturing Practice
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)