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 ...

This precision medical tubing is manufactured using process-controlled extrusion and injection molding to meet the demanding requirements of medical devices and fluidic systems. The result is tubing ...

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

The medtech industry's push into decentralized clinical trials (DCTs) has rightly focused on technology and patient diversity. 1 As part of this global shift, community health workers (CHWs) are ...

Sterilization validation is a critical step for manufacturers in the medical device, IVD, and pharmaceutical industries. Explore how Process Challenge Devices (PCDs) play a central role in ensuring ...

Ethylene oxide (EO) sterilization remains essential for medical devices, but its toxic profile and tightening regulations are driving a shift toward safer, lower-concentration cycles. This brochure ...

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

In micro-manufacturing, supplier choice significantly determines success. Explore how one company transformed a struggling ...

Selecting the right Process Challenge Device (PCD) configuration is essential for achieving reliable sterility assurance in EO sterilization of medical devices and IVD products. Gain practical ...

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 ...