Report finds medtech companies are taking new approaches as software, connected technologies, and evolving regulations gain importance throughout device life cycles.

Medical device makers in Europe are changing how they develop and manage products as software, connectivity and regulation ...

The Medicines and Healthcare products Regulatory Agency (MHRA) has published draft regulations reforming pre-market requirement for medical devices and in vitro diagnostic medical devices in Great ...

Growing volumes of electronic healthcare devices containing batteries, electronics and valuable materials such as copper, gold, lithium and ...