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Greenlight Guru Forms Regulatory Advisory Board

Greenlight Guru Forms Regulatory Advisory Board
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Greenlight Guru Announces the Formation of Its New Regulatory Advisory Board

Greenlight Guru Announces the Formation of Its New Regulatory Advisory Board Share Article Leading medical device QMS provider establishes Regulatory Advisory Board comprised of global regulatory experts Greenlight Guru is continuing to push the ideal of harmonization and industry best practices forward through the formation of our Regulatory Advisory Board. INDIANAPOLIS (PRWEB) May 27, 2021 Greenlight Guru, the leading medical device quality management software platform, today announced the formation of its new Regulatory Advisory Board (RAB), comprised of nine veteran medical device professionals. Members of Greenlight Guru’s RAB have prior experience with regulatory bodies, including FDA and EU notified bodies, and have significant medical device industry expertise with respect to regulations, standards, and requirements impacting the medical device industry.

VoxNeuro Empowers Americans to Take Control of Their Brain Health

Share: Breakthrough technology evaluates cognitive function when a brain disorder such as injury, dementia or neurological impacts of COVID-19 are suspected VoxNeuro announces the release of their software as a medical device, the Cognitive Health Assessment Management Platform™ (CHAMP), as they pave their way to the US market. With successful registration with the FDA as a Medical Device Establishment for the distribution of the CHAMP software, a Class II Exempt Medical Device, VoxNeuro is on plan to globally change the way brain health is managed and treated. CHAMP works in tandem with VoxNeuro s Cognitive Health Assessment TM to proactively track cognitive health throughout aging, and to evaluate cognitive function when a brain disorder or symptoms related to cognitive dysfunction are suspected.

Combination pack for two cancer drugs approved

Combination pack for two cancer drugs approved
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