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If devices are integral to positive patient outcomes, device partners must play an integral role to ensure regulatory ...
Biocompatibility assessment per ISO 10993 ensures medical device safety by evaluating materials, risks, and biological ...
Needles and syringes are commonly used to retrieve cell therapies from vials, posing the risk of needle stick injury. Explore ...
<p data-end="215" data-start="0">Battelle provides end-to-end medical device development services, combining engineering, regulatory, and human-centric design to accelerate innovation from concept ...
Enhancing catheter visibility under fluoroscopy, custom radiopaque filler blends improve imaging clarity without compromising ...
Thermoplastics revolutionized medical technology by replacing glass with flexible PVC. Learn how their versatility supports advanced healthcare applications, from wound care to life-saving devices.
Material selection is the foundation for every successful medical device. In addition to performance properties, each material must be suitable for processing, compatibility with other device ...
Prototype development and product concept optimization is a core expertise for Polyzen. We have nearly three decades of experience developing and optimizing a wide variety of polymer-based medical ...
As the medical device industry continues to expand, intellectual property (IP) considerations — especially those concerning patents — are critical for medical device innovators and manufacturers.
Over the past decade, patent eligibility for diagnostic technologies has become more complex. Learn three effective strategies to navigate this challenging landscape.
With ISO TR 24971:2020, the technical committee responsible for the medical device risk management standard has finally addressed the confusion around the policy for risk acceptability criteria and ...
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