The "An introduction to Risk Management ISO 14971:2019 Training Course (Apr 27, 2026)" has been added to ResearchAndMarkets.com's offering. Understand the use of risk management in the medical device ...
The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Apr 29, 2026)" training has been added to ResearchAndMarkets.com's ...
Artificial intelligence (AI) is already indispensable in the healthcare and life sciences sector. Intelligent medical devices promise nothing less than a revolution in the art of healing. With its ...
Once the risk team has been assembled, the crucial process of identifying risks must commence. The output of the risk ...
Companies and manufacturers across the globe are looking for ways to become more environmentally friendly and reach corporate sustainability goals. While eliminating medical device waste, recycling as ...
Much of the conversation about medical device cybersecurity focuses on the new Food and Drug Administration’s (FDA) revised rules for premarket submissions. These regulations changed how devices are ...
Food and Drug Administration (FDA) regulations mandate that all medical device vendors tighten their security features with processes to find and mitigate vulnerabilities. The FDA mandate is a step in ...
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