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MedTech Intelligence

As connected devices move further into mainstream, designers and manufacturers of both the devices themselves and the software that supports them must ensure due diligence, effectiveness, as well as regulatory compliance protecting the end user’s data. Industry, FDA and customer confidence must be addressed early and often to create an on-going dialogue of how data is being protected. Read more in this EAS authored article published in MedTech Intelligence.

Posted in EAS in Action, EASeNews, Medical Devices.