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Managed Device Attestation enables enterprises to verify Apple devices for security, protecting the corporate network. Here's how to use it.

Managed Device Attestation enables enterprises to verify Apple devices for security, protecting the corporate network. Heres how to use it.

More than five years after FDA first announced its plan to harmonize 21 CFR Part 820 with ISO 13485, on February 2, 2024, FDA finally issued the Quality Management System Regulation (QMSR) Final Rule.

If you've just unboxed your brand-new Google Pixel 8 Pro, you're probably eager to dive in and explore all its features. But before you get lost in the

Food and Drug Administration FDA published a Warning Letter to RightEye, LLC RightEye manufacturer of RightEye Vision System, for misbranding and adulteration. RightEye Vision System is a Class II Nystagmograph medical device which is cleared under its 510k.

On January 31, 2023, the U.S. Food and Drug Administration (FDA) published a Warning Letter to RightEye, LLC (RightEye), the manufacturer of the RightEye Vision System, for misbranding...

/PRNewswire/ -- The "Brain Monitoring: Global Market Outlook" report has been added to ResearchAndMarkets.coms offering. In this report, the market has been...

The Medicines and Healthcare products Regulatory Agency (the MHRA) consulted on proposed changes to the UK’s regul…

The FDA has issued two separate draft guidance documents for medical devices being marketed subject to 1) an Emergency Use Authorization and 2) enforcement discretion ...

FDA’s Center for Devices and Radiological Health has published two draft guidance documents in anticipation of the end of the public health emergency brought about by the COVID-19 pandemic. Devices subject to the guidances should consider reviewing these documents carefully.