What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
A recent study identified 157 cardiovascular devices recalled from 2013 to 2022. Recalls were commonly attributed to device ...
HeartBeam has submitted a 510 (k) application to the US Food and Drug Administration (FDA) for its 12-lead electrocardiogram ...
Mass., grilled Robert F. Kennedy Jr. over his plans to profit off of drug companies or lawsuits after being Health and Human ...
The "FDA Inspections: From Site Preparation to Response" training has been added to ResearchAndMarkets.com's offering. This is a practical, hands-on two-day seminar designed to provide pharmaceutical, ...
Several ASX-listed companies are undertaking phase III clinical trials, the critical final stage before potential regulatory ...
Meanwhile, in an executive order, Trump created his long-discussed “Department of Government Efficiency,” to be led by Elon ...
The FDA submission is backed by robust data from the VALID-ECG pivotal study, which enrolled 198 patients across five clinical sites. The Company believes the study's findings support the clinical ...
Many companies and investors believe that AI has to potential to reshape various elements of the pharma industry. Two ...
ColdVest is a patented FDA Class 1 medical device designed to rapidly lower core body temperature, preventing heat stroke and ...