STEMart, a US-based provider of comprehensive services for all phases of medical device development, proudly announces the launch of its new Sterile Barrier & Seal Integrity Testing services for medical device manufacturers to optimize packaging design and performance. This suite of tests ensures the safety and efficacy of medical devices by guaranteeing the integrity of their packaging throughout processing, distribution, and storage. Medical devices, pharmaceuticals and other healthcare pro...

STEMart, a US-based provider of comprehensive services for all phases of medical device development, is proud to announce the launch of its new Pilot Production Services for the medical device industry. These services allow manufacturers to test and refine their products prior to full-scale production, streamlining the development process of new medical devices and minimizing risk to save time and costs. Pilot production is the process of manufacturing a device using a process that is close t...

STEMart, a US-based provider of comprehensive services for all phases of medical device development, proudly announces the launch of its new Medical Device Prototyping Services. Using the latest technologies, these reliable prototyping solutions can help medical device companies streamline the development process and test new products quickly and cost-effectively, saving time and resources. Prototyping is the process of creating a primary version of a product for visualization and conceptuali...

STEMart, a US-based provider of comprehensive services for all phases of medical device development, announced the launch of its new Force Degradation Services to help pharmaceutical and medical device companies evaluate the stability of their drug candidates and finished products under a variety of stress conditions, ensuring their safety and efficacy throughout their shelf life. Forced degradation studies are used to demonstrate the molecular chemical behavior of processed products that may...

STEMart, a US-based provider of comprehensive services for all phases of medical device development, has announced the launch of its Disinfection Efficacy Studies Services in various standards to ensure the safety of medical devices. The services can be performed to evaluate the effectiveness of disinfectants against a wide range of microorganisms, including bacteria, yeast, viruses, and fungi. Good Manufacturing Practices (GMP) regulations and FDA guidelines require biologic/pharmaceutical m...

STEMart, a US-based provider of comprehensive services for all phases of medical device development, has announced the launch of its Rapid Endotoxin Testing Services to help medical device manufacturers quickly and accurately assess the endotoxin levels in their products. Bacterial endotoxins are lipopolysaccharides (LPS) bound to the bacterial cell wall and released when the bacteria rupture or break down. They consist of three major components, O antigen, core oligosaccharide, and lipid A m...