Medical Blog

From the Editor - AI: A “Transformative Force” in Medtech, But Hurdles Remain

AI is poised to make a major impact on the medtech market by enhancing precision in diagnostics, personalizing treatment plans, and streamlining manufacturing processes. Read on to find out what Editor and Director of Medical Content Sherrie Trigg thinks about the matter.

Making EVs Accessible for All

To address the needs of wheelchair accessible vehicle (WAV) users in the U.K.’s transition to electric, Motability Operations has revealed eVITA. It’s an accessible and versatile concept electric wheelchair accessible vehicle (eWAV), designed in collaboration with CALLUM.

Space Station Germ Testing Improves Wastewater Monitoring

A technology developed for NASA to identify pathogens inside spacecraft turned out to be beneficial for wastewater surveillance on Earth.

From the Editor - FDA Releases Draft Guidance for Drug-Delivery Devices

At the end of June, FDA released a draft guidance that is designed to facilitate and streamline development of stand-alone devices and combination products by improving the consistency of drug-delivery performance information included in applications and submissions. Read on to learn more about it.

The Politics of Health: How Global Elections Will Impact on Life Sciences

The global landscape for medical technology, biotechnology, and life sciences is on the cusp of seismic change.

AI + Computer Simulations = Enhanced Robotic Exoskeletons

Researchers have demonstrated a new method that leverages artificial intelligence (AI) and computer simulations to train robotic exoskeletons to autonomously help users save energy while walking, running, and climbing stairs.

From the Editor - Medical Robotics: Report Reveals Clinician Expectations

From the Editor discusses Robocath -- a company that designs, develops, and markets innovative robotic solutions to treat cardiovascular and neurovascular diseases -- and how it has published a new report exploring current and future expectations for the use of robotics in interventional medicine. Read on to learn more.

Guest Editorial

This editorial was written by Ivor Campbell, Chief Executive of Callander, UK-based Snedden Campbell, a specialist recruitment consultant for the medical technology industry. He talks about who holds the key to the future of public health diagnostics. Read on to learn more.

Imperceptible Sensors Printed Directly on Human Skin

Researchers have developed a method to make adaptive and eco-friendly sensors that can be directly and imperceptibly printed onto a wide range of biological surfaces.

From the Editor - Advances in Generative AI to Reshape Healthcare

Generative artificial intelligence (or genAI) is rapidly gaining traction in the healthcare and pharmaceutical domains, with substantial advancements helping to address pervasive issues in these industries.

From the Editor - Surge in Metal AM Systems Drives Growth in 3D Printing

Shipment of additive manufacturing (AM) systems for metal parts increased by 24.4 percent in 2023, according to Wohlers Associates latest report. See what Editor and Director of Medical Content Sherrie Trigg thinks about the matter.

From the Editor - Study: The Post-COVID Impact of 3D Printing and Generative Design

As the COVID pandemic began to drive rapid changes in healthcare, innovative manufacturers and makers around the world began using 3D printing and generative design to fill a dire need for masks, swabs, ventilator components, and other medical equipment. Read on to learn more thoughts from Sherrie Trigg, Editor and Director of Medical Content.

From the Editor: The 2023 Products of the Year

This year, our two winners both focus on materials designed to address the special needs of the healthcare industry. Read on to learn the winners of the 2023 Medical Design Briefs’ Readers’ Choice Products of the Year.

From the Editor - Minimal Link Between Device Value and Device Purchasing

There is sparce evidence in the health research literature to link health technology assessment (HTA) processes and outcomes (at a national, regional, or hospital level) with device purchasing decisions, according to ISPOR. Read on to learn new findings and more.

From the Editor - FDA's LDT Regulation Must Balance Safety and Innovation

Analytics firm GlobalData has weighed in on the U.S. FDA's proposal to reclassify laboratory-developed tests (LDTs) as medical devices. FDA historically exercised enforcement discretion over LDTs, meaning that it did not actively regulate them like it does for other medical devices, so this is a significant regulatory change.

Q&A: Implementing Advanced Medtech Manufacturing

The advent of Industry 4.0 marks a transformative change in the manufacturing landscape, presenting abundant prospects for enhanced efficiency, personalized solutions, and groundbreaking...

The Impact of Cybersecurity Within the Healthcare Industry

New tools and technologies are driving healthcare change. The rapid adoption of mobile applications, cloud solutions and wearable devices makes it possible for care professionals to...

From the Editor - AI Medical Imaging Products Could Increase Five-Fold by 2035

Assuming that future funding follows the same linear trend that it has previously, a study projects such funding will be $30.8 billion in 2029, which would lead to FDA-approved products in 2035.

Active Implantables: Put Design at the Heart of the Process

Implantable medical devices may be nothing new — doctors have been inserting things like pacemakers and cochlear implants into their patients’ bodies for decades — but as the relationship between people and technology becomes ever more co-dependent.

From The Editor: The Art of Finding the Perfect Color for Medical Devices

The selection of colors for medical devices can be a complex process that takes into account various factors, including functionality, safety, aesthetics, branding, and regulatory requirements. But where do you start? See what Editor and Director of Medical Content Sherrie Trigg says.

The Consultant, the FDA, and You

Understanding what the FDA really means by their time frames, knowing how to address their regulatory issues, and preparing a response to a 483 or Warning Letter is critical to showing the FDA that you understand what they expect from you and that you will work to bring your company into compliance. Another critical point is to understand that you can negotiate with the agency.

A Flexible Future: Market Analysis of Flexible Packaging for Healthcare

The healthcare sector is always changing with new advancements and approaches emerging. One area that has experienced progress in recent times is flexible packaging....

From the Editor - Where to Go to Grow Your Medtech Start-Up

Where are the medtech opportunities in the future? Find out from Editor and Director of Medical Content Sherrie Trigg the markets with top-10 life sciences talent pools.

Guest Editorial

Written by Katie Falcone, Scientific Support Manager, Datwyler, this article addresses the dangerous implications of micro material contamination.

Q&A: Implications of Industry 4.0 and the Future of Manufacturing Automation

Industry 4.0 is bringing about a fundamental shift in manufacturing, offering numerous opportunities for efficiency, customization, and innovation. This Fourth...

From the Editor - How One Company Is Using AI to Disrupt Traditional Medtech

Proprio, a Seattle-based surgical technology company, achieved a significant milestone this year when its flagship surgical navigation platform, Paradigm™ obtained FDA 510(k) clearance.

Guest Blog: AI, Robots, and Nanotech — Study Examines What's Acceptable in Healthcare

A new study provides interesting insights into the public's perception and acceptance of AI, robots, and nanotech in the healthcare industry, shedding...

From The Editor - Patient Demand Drives Smart Drug-Delivery Systems Market

A recent report reveals that the growth in prevalence of chronic diseases and rise in patient preference for advanced drug-delivery systems are driving the global smart drug-delivery systems market.

From the Editor - How 3D Printing Could Improve Spinal Surgery

Medical device company Mighty Oak Medical recently announced a technical partnership with HP for 3D printed healthcare applications to improve pedicle screw placement in spinal procedures.