Infographics can propel MedTech research and campaigns and enhance the user experience. Here Fabricio Pamplona, co-founder of online infographic maker for scientists Mind the Graph, explores the power ...

A review of common risks and pitfalls of incorporating artificial intelligence in medical devices and an overview of the regulatory framework.

Titanium has become a vital material in modern medicine due to its strength, light weight, corrosion resistance, and exceptional biocompatibility with high long-term success rates and minimal risk of ...

Wes Sonnier serves as the President of BioMedical Waste Solutions. With a deep-seated commitment to environmental responsibility and innovation, Wes has been instrumental in steering the company ...

It looks at the rise of fraudulent research and scientists in the life sciences industry, the reasons for the rise, and suggests some measures that companies can take to counter this growing threat to ...

Evolving regulations and market requirements have kept medtech companies on their toes for years. EU MDR, for example, has been a top priority and now, more companies are moving toward EU MDR ...

Several alternatives exist to obtain FDA approval of artificial intelligence-enabled medical technology. Determining the best approach for a new device will require an awareness of each pathway’s ...

As technology component pricing continues to rise, MedTech manufacturers are applying proven methods and exploring new approaches to maintain profitability and extend product lifecycles.

A global need for less invasive medical procedures and high efficacy treatments has outlined the developments of cardiovascular devices.

The application of AI in telehealth to allow doctors to make real-time, data-driven rich choices is a key component in generating a better patient experience and improved health outcomes.

The Department of Veterans Affairs (VA) and the Department of Defense (DoD) present very attractive markets to a wide range of medical device and supply providers. However, with more than 18 million ...

New directives and guidance aim to connect patients, physicians and other stakeholders across the healthcare ecosystem with a consistently up-to-date information source for product and safety ...