Market opportunities include comprehensive training on ISO 10993 standards compliance, essential for meeting EU Medical Device Regulation safety requirements. This course equips participants with risk ...

In the evolving global healthcare procurement system, the demand for a China OEM medical device supplier has increased significantly as hospitals, distributors, and rehabilitation institutions seek ...

After Israel tightened requirements for aid entering Gaza, a Houston nonprofit found a way to send medical supplies by ...

Today, Senators Jim Banks (R-Ind.) and John Hickenlooper (D-Col.) introduced the Medical Device Electronic Labeling Act. This ...

Patent-Pending Handheld Breathomics Platform Designed to Help Consumers Understand Metabolic Wellness, Lifestyle ...

Dukane partnered with a medtech manufacturer to develop ultrasonic welding processes for a new CGM device designed to support ...

The European Parliament and Council have reached a provisional agreement on the Critical Medicines Act (CMA), moving ...

The International Medical Device Regulators Forum (IMDRF) has released a guidance for manufacturers on how to choose, ...

For manufacturers, medical device companies, and laboratories that use the commercial diagnostic tests they produce, ...

The Centers for Medicare & Medicaid Services (CMS) and the Food and Drug Administration (FDA) recently issued two related proposals that, taken together, would significantly alter the pathways ...

Opinion: The EPA's proposed amendments to the National Emission Standards for Hazardous Air Pollutants for commercial ...

With its reform proposal to the Medical Devices Regulation (MDR; COM(2025) 1023 final) presented on 16 December 2025, the ...