Vivani Medical Cofounder and CEO Adam Mendelsohn, Ph.D. discusses the company’s first application of the NanoPortal, ...

Article 16 of the European Union’s Medical Device Regulation and In Vitro Diagnostic Regulation specifically address the ...

In the medical device industry, FDA inspections are not a regulatory hurdle — they are a powerful tool for improving product quality, operational efficiency, and patient safety. Shift from a reactive ...

Experience the next generation of biopharma innovation with PharmaLok™ ZerO sanitary clamps. Designed to simplify and streamline biopharma processes, these advanced clamps feature a universal fit and ...

The rapid evolution of telehealth is transforming how patients access — and physicians provide — care, a shift accelerated by policy changes adopted during the COVID-19 pandemic. The announcement in ...

The updated requirements for post-market surveillance (PMS) under the EU Medical Device Regulation (MDR), EU In Vitro Diagnostics Regulation (IVDR), and the U.K.'s forthcoming Statutory Instrument (SI ...

The Royal Master Centerless Grinders are ideal machines for grinding catheter bodies. With our TG 12x3 and TG 12x4 Models, one has the ability to hold close, consistent diameter tolerances along the ...

Plastics are used in many of today’s medical devices because of the wide range of materials and properties available to match the device requirements. In addition to being lightweight, plastics can be ...

Quality Management Software - CATSWeb is not just a static data repository, it's a collaborative, real-time dynamic workflow tool that assists you in your problem solving efforts. This software will ...