A European medical distributor improved healthcare delivery by introducing a portable hemoglobin meter to pharmacies, clinics, and hospitals — boosting diagnostic speed and patient care.

When routine quality inspections uncovered non-conforming products at a partner factory, we refused to compromise. Discover how our team’s relentless advocacy secured a 12% compensation for our client, proving that true partnership means defending quality at every step – even when facing resistance.

The 91st CMEF 2025, As a key industry player, MedAsia Healthcare showcased its three core business pillars—home diagnostic test strips, household health monitoring devices, and customized service plans—under the theme “Intelligent Global Healthcare, Co-Creating a Healthy Future”

QMSR wird das Qualitätsmanagementsystem für Medizinprodukte der FDA an ISO 13485:2016 anpassen. Es wird bis Ende dieses Jahres veröffentlicht und tritt ein Jahr später in Kraft. Es wird erwartet, dass diese Harmonisierung den Medizintechnikunternehmen in den nächsten zehn Jahren mindestens 439 Millionen US-Dollar einsparen wird.

With tightening EU regulations like MDR, IVDR, RoHS, and REACH, medical importers and distributors face growing compliance and supply chain risks. This article explores key impacts, actionable steps, and how working with Medasia ensures access to certified, cost-effective, and regulation-ready medical products.

As EU MDR/IVDR and environmental rules tighten, importers face growing compliance demands. This article highlights key 2024–2025 regulatory updates, their impact on importers, and offers practical guidance for compliant sourcing and market access.