Learn more about the critical tests for ensuring the proper performance of auto-injectors, which are used for a variety of ...

Cleanroom micro molding ensures ultra-small components meet strict contamination and performance standards. As devices shrink ...

Liquid Silicone Rubber (LSR) is redefining optical micro molding with superior durability, design flexibility, and thermal ...

Establishing combination product shelf life requires aligning stability. Holistic, data-driven stability studies ensure ...

Ready to improve your submission success rate? Define clear submission goals, ensure cross-functional collaboration, and ...

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.

Vascular devices face mounting design and manufacturing challenges. Explore how hybrid material strategies and integrated expertise are helping developers balance performance, scalability, and ...

Connected medical devices must treat Protected Health Information (PHI) protection as integral to patient safety and ...

Managing global PFAS regulations demands a proactive strategy. Identifying and mitigating both intentional and unintentional ...

An FDA warning letter is more than a formal notice; it’s a visible sign that a company’s quality system has failed to meet critical expectations. Yet behind every warning letter lies a wealth of ...

The global medical device market is estimated to be currently about $680 billion and is projected to grow to over a trillion dollars within 10 years at a compound annual growth rate of 6%. 1 As the ...

The U.S. Food and Drug Administration (FDA) has issued its much-anticipated final guidance on cybersecurity risk management in medical devices, effective June 2025. This document, titled ...