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The Medical Device Regulation (MDR) has significantly reshaped the regulatory landscape in the European Union. With multiple deadlines, ongoing challenges, and growing concerns among industry experts, the transition remains a complex process for manufacturers. Here’s a comprehensive look at the...

Introduction Adaptive designs have revolutionized clinical trials, especially in medical device development. These designs allow preplanned modifications based on interim data, maintaining the integrity and validity of the study while enhancing flexibility and efficiency. The U.S. Food and Drug Administration...

Find out how to join us in Düsseldorf! We are excited to announce that we are preparing to exhibit at COMPAMED 2024, one of the world’s most prestigious medical technology and innovation trade fairs, which will take place in Düsseldorf,...

Bringing a medical device to market in the United States requires navigating a complex regulatory landscape, primarily regulated by the Food and Drug Administration (FDA). Understanding the classification, regulatory pathways and compliance requirements is critical to success. At D.med Technologies,...

Introduction to Vital Signs measurement Vital signs are the essential indicators of the body’s basic functions, reflecting the state of an individual’s health. Monitoring these signs is crucial in medical settings to assess the immediate and long-term health status of...

D.med Technologies invites all attendees of MedtecLIVE 2024 to visit stand 1-543 to learn more about our services and how we can help you bring your medical devices to market. 18-20 June 2024.Messe, Stuttgart. This is a great opportunity for...

this is the Excerpt. The last decades have been surrounded by many cybersecurity attacks around the world, many of them in Hospitals or Medical Devices. For example, on September 12th, 2022, the FBI warned that many medical devices with outdated...