Recent high-profile failures and recalls of medical devices highlight concerns about patient safety. Robotic automation in ...

The MD series medical-grade capacitors ensure high reliability for implantable devices, offering screened and unscreened options to streamline prototyping and production for medical device designers.

Gain an understanding of PFAS, their properties, environmental impact, health risks, and regulatory challenges, focusing on ...

The U.S. market is continuing its shift away from traditional wound dressings (gauze, tape, etc.) toward advanced wound care ...

The pharma industry has invested greatly in IT systems and optimized data and content management. Medical device companies can learn from pharma's experience — and it will ease the regulatory burden.

Medical device companies can live and die by the 510(k) process. It lets the market know that the device is safe and effective, and it protects users from liability if the device doesn't perform as ...

Developing generic drug-device combination products (g-DDCPs) is a complex and time-consuming process that often requires extensive clinical trials and regulatory submissions. However, a new six-phase ...

Recently, Latin America has emerged as a promising frontier for medical device clinical trials, with Chile at the forefront of this development. The country's robust healthcare infrastructure and fast ...

VitalDose® EVA technology offers a patient-centric approach to women's health therapies. By enabling controlled, long-acting release of diverse molecules, including small molecules, peptides, RNA, and ...