Gotechtor on MSN

Apple is cutting 16 devices from software support this fall — including a $799 watch it sold 4 years ago

Apple drops 16 devices this fall, including five Apple Watches at once. Find out if your device is affected and what happens ...
RAPS

Medical device software regulations in the EU and US

Software-based medical devices are integral to healthcare. To enter the marketplace, a company must successfully navigate and comply with applicable national and international regulatory requirements.
MD&M East

Validating Software as a Medical Device (SaMD)

Software in the healthcare industry has come a long way over the past 20 years. Medical device companies, like most life sciences companies, were a bit hesitant to incorporate software and automation ...
MD&M East

Software User Interface Requirements for Medical Devices

Medical devices have to be designed so that people can use them easily and reliably. Human factors considerations have gained increased attention since the release of FDA's guidance document, Medical ...
Bleeping Computer

Mobile device management done right: Top MDM tools to secure your devices

Mobile device management creates a standard setting for corporate owned mobiles, tracks their location, and enforces security. Systems can also manage BYOD. Find out the best MDM system. Businesses ...
Nature

Beyond the 510(k): The regulation of novel moderate-risk medical devices, intellectual property considerations, and innovation incentives in the FDA’s De Novo pathway

Medical devices have played a critical role in raising the standards of healthcare delivery. The COVID-19 pandemic underscored clinical medicine’s dependence on devices ranging from diagnostic test ...
Forbes

What Is IoT Device Management? Definition And Best Practices

Kimberlee Leonard has 22 years of experience as a freelance writer. Her work has been featured on US News and World Report, Business.com and Fit Small Business. She brings practical experience as a ...
JD Supra

Coverage of FDA’s AI/ML Medical Devices Workshop - Part 1: The History of FDA Software Regulation

In anticipation of FDA’s virtual public workshop on transparency of artificial intelligence/machine learning (AI/ML)-enabled medical devices scheduled for October 14, 2021, we will be posting a series ...
Nature

FDA-authorized software as a medical device in mental health: a perspective on evidence, device lineage, and regulatory challenges

FDA approval is widely regarded as a benchmark of quality for medical devices. However, concerns persist regarding its regulatory framework for digital mental health devices. This perspective article ...
InfoWorld

How to deploy software to Linux-based IoT devices at scale

Deploying software to large fleets of Linux-based devices is a complex and critical process that requires careful planning and automated execution. Start with these best practices. The internet of ...
ISA

Focus on HART Devices and Software

The 154 HART calibration assistant is a standalone tablet-based communication tool for HART configuration. The 154 provides HART communication functionality. When combined with a 750 series ...