Brazil is rapidly establishing itself as a powerhouse in medical device innovation. This article shares market opportunities, ...

If devices are integral to positive patient outcomes, device partners must play an integral role to ensure regulatory ...

<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 ...

Sterilization validation ensures medical device safety by confirming sterility through rigorous testing, method selection, ...

USP 382 introduces system-level, function-specific testing for elastomeric components in parenteral packaging, improving ...

Needles and syringes are commonly used to retrieve cell therapies from vials, posing the risk of needle stick injury. Explore&nbsp;the suitability of needle-free polycarbonate&nbsp;transfer devices.

Biocompatibility assessment per ISO 10993 ensures medical device safety by evaluating materials, risks, and biological effects, emphasizing rigorous risk management, updated standards, and reduced ...

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 ...

The digital revolution that resulted in the IoT, IoMT, SaMD, and connected devices comes with the possibility of cyberattacks. The FDAs latest efforts to enhance medical device cybersecurity include a ...