MvPI releases draft IVD-MD adverse event reporting form, invites stakeholders' comments till March 5: Our Bureau, New Delhi Thursday, February 20, 2025, 08:00 Hrs [IST] The Materi ...

to In Vitro Medical Devices Regulation (EU) 2017/746 (IVDR). Historically, IVD devices could be self-assessed under the 1998 Directive, meaning that manufacturers could declare that the device was ...

Medical devices comprise electronic equipment, implants, consumables and disposables, surgical instruments and in-vitro ...

In vitro fertilization (IVF) is a medical procedure that helps people facing infertility build their families.

an in vitro diagnostic medical device that harnesses AI to generate heatmaps identifying small and rare missed prostatic cancers, acting as a safety net that assists pathologists in ensuring patients ...

Emboa Medical has developed a novel blood clot extraction device to address the prevalent issue of stroke, which is the second leading cause of death in the world. Using nature-inspired design, Emboa ...

The goal is to improve patient safety by monitoring, recording, and analysing the root cause of adverse events or risks associated with the use of medical devices, including in-vitro-diagnostics.