Newsletter | March 14, 2024

03.14.24 -- 6 Things Medtech Companies Should Know About The EU's AI Act

FEATURED EDITORIAL

6 Things Medtech Companies Should Know About The EU’s AI Act

With the recent publication of the European Union’s long-awaited Artificial Intelligence Act (AI Act), the message to medtech companies is clear: you need to move toward compliance by understanding your AI systems, determining their role under the AI Act, and identifying the specific obligations and implementation strategies that apply.

INDUSTRY INSIGHTS

10 Ways To Align Your Medical Device With Human Factors Best Practices

Discover how patient-centric design principles can improve the development of medical devices. By focusing on user needs and behaviors, manufacturers can ensure that products align with expectations.

Why Perform A Product D-Value Study?

Follow our discussion on nonheat sensitive aqueous liquid product sterilization and the use of the Overkill method and Bioburden/BI method.

Snubber Capacitors In The Field

Learn about the changing landscape of power supply circuits and why it's important to adapt to advancements in semiconductor technology.

Reducing Human Error In Healthcare Operations And Equipment Management

Implementing an IoT platform powered by RFID enables clinicians to effectively use medical equipment and reduce human error in healthcare processes to ensure higher quality of care.

CM Partnering For Adaptable, Accelerated Market Acceptance

The need for manufacturing support that offers adaptable, scalable solutions has become more crucial than ever for the diagnostic space.

ARTICLES YOU MAY HAVE MISSED

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A Data-Derived Approach For Selecting Criticality Levels In FMECAs For Cleaning Process Risk Analysis

Understanding Australia’s Regulatory Framework For SaMD

Use-Related Risk Analysis For Combination Products

5 Focus Areas For Medtech Business Success In 2024

RESOURCES

Medical-Grade Polyethylene Fibers: Ulteeva Purity

Premium Grades For Orthopedic Implants: GUR UHMW-PE

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