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
By 2050, there will be around 83.7 million senior citizens in the United States, increasing rapidly from 49.2 million in 2016. The ageing population across
In these two case studies, Sanmina’s expertise in manufacturing technologies for medical devices, as well as experience with this highly regulated market sector helped two
