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”

By 2025, medical device importers and distributors will face one of the most significant regulatory shifts in decades. The European Union's MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) deadlines are closing in, while the U.S.

QMSR приведет систему управления качеством медицинских изделий FDA в соответствие с ISO 13485:2016. Он будет выпущен к концу этого года и вступит в силу через год. Ожидается, что эта гармонизация сэкономит компаниям, производящим медицинские устройства, не менее 439 миллионов долларов в течение следующего десятилетия.

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.