The E2MS specialist increases its presence at the exhibition Livingston – Plexus Corp., a global provider of electronic engineering and manufacturing services (E2MS), will exhibit at the 2018
It is difficult to manufacture minimally invasive devices to the quality standards required for Class III medical devices. That’s not to say it can’t be
With a 2020 deadline looming for the European Union’s Medical Device Regulation (MDR), regulatory affairs and quality leaders at medical device makers lack understanding of
KPMG, Regulatory Affairs Professionals Society Survey Finds a Lack of Understanding about EU MDR and concerns about clinical data collection. With a 2020 deadline looming
The potential applications of wearables are plentiful and diverse. Thanks to progress in miniaturization, smart devices can be weaved into clothing, implanted in shoes or
