Proving your product to be safe and effective while also getting buy-in from the healthcare ecosystem are only some of the ...
A study has found that nearly a third of medical device AEs were reported by manufacturers later than FDA's required 30-day ...
New leadership often means new regulations for government, which can create uncertainty for cybersecurity teams that manage and protect vast networks of devices. Automation is one way to streamline ...
Dr. Dina Radenkovic, CEO of Gameto, discusses the key considerations for bringing iPSC-based fertility treatments to market from a regulatory and manufacturing perspective.
Following the success of its initial deployment, Andelyn is now expanding microsegmentation policies to additional sites and ...
In the ever-evolving landscape of industrial safety, vigilance and adaptability are key. By leveraging the latest ...
The UK Government has accepted most of the recommendations of the Regulatory Horizons Council (RHC) on the regulation of AI in medical devices.
Proposed amendments would forbid the use of all personal electronic devices during school hours in high schools and below, ...
The National Association of Boards of Pharmacy (NABP) plays an important role in the state licensing of prescription medical device manufacturers ...
Last year, the EPA issued a final rule that would limit emissions of ethylene oxide, a cancer-causing gas used to sterilize ...
Homebuyer demand is increasingly moving from ready-to-move-in (RTMI) properties to newly launched or under-construction (UC) ...
A comprehensive and forward-looking regulatory framework for emerging technologies can address integration challenges, ...