New Report Expects AI to Drive Revenue Management Value in 2025
Model N’s 2025 State of Revenue Report reveals shifts toward the use of generative AI and automation to bolster medtech and high-tech revenue programs.
Packaging for Med Device Companies: EO and CD Considerations
What medical device manufacturers should keep in mind when packaging for chlorine dioxide (CD) versus ethylene oxide (EO).
2024: Emerging Trends Shaping the Future of Healthcare
In the rapidly evolving landscape of healthcare, the integration of technology is driving a transformative shift. As industry navigates these technological frontiers, the collective goal is to enhance patient experiences, streamline processes, and make healthcare more accessible and equitable. This article explores key emerging trends that are not only improving patient engagement but are also set to redefine the future of healthcare.
2024 Predictions for Medical Packaging
What medical packaging trends are most likely to garner attention in 2024? Packaging Digest explored this during a virtual roundtable with industry experts.
What 1988 Event Impacted the Use of Luer Connectors?
By 1980, the luer connector had become standard in the United States for connecting catheters to plastic tubing, according to a detailed history of the luer that MD+DI published in 2012. In Europe, however, the Record (also known as Rekord) was most widely used.
FDA Encourages Vaporized Hydrogen Peroxide as Possible EtO Alternative
The U.S. Food and Drug Administration (FDA) announced that it considers vaporized hydrogen peroxide (VHP) to be an “established method of sterilization” for medical devices.
Preserving Critical Manufacturing Supply Through Digital Stockpiles
FDA and VHA have partnered to create digital stockpiles that store electronic plans, instructions, and methods to make and test medical products.
Stabilization in Medtech: Are We There Yet?
Here’s what medtech executives are seeing this year in terms of procedure volumes, supply chain pressures, and hospital staffing challenges.
The Bumpy Road to MDR
As one of the most impactful regulatory updates to the EU medical device market in recent years, the European Union’s Medical Device Regulation 2017/745 (MDR) has been a hot topic of conversation since it entered into force in May 2017.
How a 1969 Battery Ad Inspired a Medical Device Invention
The year was 1969 and Robert Fischell was lying on the couch in his living room, reading IEEE Spectrum, a magazine published by the Institute of Electrical and Electronics Engineers, when he saw an advertisement that would lead to one of the world’s greatest medical device inventions.
