Visit Medbio at Booth #941, November 19–20, to explore custom injection molding and assembly solutions, supporting Class I–III devices with quality, compliance, and MedTech innovation.
The medtech industry desperately needs — and currently lacks — a practical trial-specific financial framework to build a ...
Vascular devices face mounting design and manufacturing challenges. Explore how hybrid material strategies and integrated expertise are helping developers balance performance, scalability, and ...
Managing global PFAS regulations demands a proactive strategy. Identifying and mitigating both intentional and unintentional ...
In micro-manufacturing, supplier choice significantly determines success. Explore how one company transformed a struggling ...
This in-depth article describes risk in cleaning and provides a science- and risk-based framework for selecting analytical methods using ASTM International standards. Here are practical tips to build ...
Current risk analysis methods focus on the possibility and severity of bad events instead of focusing directly on analyzing and improving the performance of systems and processes producing the bad ...
In medical device manufacturing, precision isn’t optional—it’s mandatory. Yet many teams still rely on paper-based processes or rigid legacy MES platforms that slow down innovation and complicate ...
One major change introduced by the Regulation (EU) 2017/745 (Medical Device Regulation [MDR]), compared to the former Directives 90/385/EEC (Active Implantable Medical Device Directive [AIMDD]) and 93 ...
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