Medical Blog

Join the conversation! Medical Design Briefs' Editor Sherrie Trigg provides her take on today’s innovative technology developments and the topics most important to you.

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From the Editor: Medical
Hear directly from Sherrie Trigg, Editor and Director of Medical Content, about the FDA's final ruling on LDTs and why that is raising concern.
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From the Editor: Design
Gen AI is an impressive technology with seemingly limitless applications. We’ve barely begun to scratch the surface of what it can do. But it’s this very limitlessness that makes it a poor fit for use inside of a medical device. Read on to learn more.
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From the Editor: Medical
A new report has found that 36 percent of Americans admit they would continue to use products even after a recall. See what Sherrie Trigg, Editor and Director of Medical Content, has to say about the use of recalled products and future loyalty.
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From the Editor: Robotics, Automation & Control
The global market for robotic surgical systems and their accessories will reach $10 billion in 2024, with a substantial increase expected to $15.8 billion by 2030. Read on to learn what Sherrie Trigg, Editor and Director of Medical Content, has to say about surgical robots.
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Blog: Medical
The environmental impact of the healthcare industry has been widely reported, with estimates it is responsible for around 4–5 percent of total global greenhouse gas emissions.1 As...
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Blog: Medical
Recently, I came across an FDA regulatory situation you do not see too often. On the same day, FDA sent two teams of field investigators into two geographically different sites of the same company to...
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From the Editor: AR/AI
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.
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Blog: Power
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.
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NASA Spinoff: Aerospace
A technology developed for NASA to identify pathogens inside spacecraft turned out to be beneficial for wastewater surveillance on Earth.
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From the Editor: Regulations/Standards
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.
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Blog: Regulations/Standards
The global landscape for medical technology, biotechnology, and life sciences is on the cusp of seismic change.
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Blog: Medical
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.
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From the Editor: Robotics, Automation & Control
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.
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From the Editor: Medical
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.
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Blog: Medical
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.
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From the Editor: AR/AI
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.
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From the Editor: Manufacturing & Prototyping
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.
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From the Editor: Medical
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.
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From the Editor: Medical
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.
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From the Editor: Medical
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.
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From the Editor: Regulations/Standards
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.
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Blog: Medical
The advent of Industry 4.0 marks a transformative change in the manufacturing landscape, presenting abundant prospects for enhanced efficiency, personalized solutions, and groundbreaking...
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Blog: Connectivity
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...
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From the Editor: Imaging
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.
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From the Editor: Medical
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.
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From the Editor: Design
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.
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Blog: Regulations/Standards
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.
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Blog: Medical
The healthcare sector is always changing with new advancements and approaches emerging. One area that has experienced progress in recent times is flexible packaging....
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From the Editor: Manufacturing & Prototyping
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.
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Ask the Expert

Ralph Bright on the Power of Power Cords
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Understanding power system components and how to connect them correctly is critical to meeting regulatory requirements and designing successful electrical products for worldwide markets. Interpower’s Ralph Bright defines these requirements and explains how to know which cord to select for your application.

Inside Story

Inside Story: Trends in Packaging and Sterilization
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Eurofins Medical Device Testing (MDT) provides a full scope of testing services. In this interview, Eurofins’ experts, Sunny Modi, PhD, Director of Package Testing; and Elizabeth Sydnor, Director of Microbiology; answer common questions on medical device packaging and sterilization.

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