STEMart, a US-based provider of comprehensive services for all phases of medical device development, recently announced its the launch of its comprehensive Flow Cytometry Services to meet the diverse needs of research, diagnostics, and clinical studies, o...

STEMart introduces Balloon Catheter Testing Services for the development of safe and effective medical devices.

CD Bioparticles launches new line of Agonist-Based Adjuvants to support researchers.

CD Bioparticles announces its new Endotoxin Free Gold Nanoparticles for biomedical research and bioassay development.

STEMart announces the expansion of its services to include comprehensive Altitude Testing.

STEMart announces the launch of its new Real-time Aging Testing services.

STEMart announces the launch of its new Transportation and Distribution Simulation Services for the medical device industry.

STEMart announces the launch of its Packaging Solutions for the pharmaceutical and medical device industries.

STEMart proudly announces the launch of its new Medical Device Prototyping Services.

An antimicrobial or preservative is defined as a chemical substance that will kill microorganisms or inhibit the growth of microorganisms, usually added to nonsterile products to protect them from microbiological contamination.

A microbiological potency assay measures the bioactivity or potency of an antibiotic by the degree of growth repression on susceptible microorganisms at different concentrations.

Biocompatibility evaluation of breathing gas pathways in medical devices is a powerful tool for the evaluation of contaminants from the air emitted from the device for Volatile Organic Compounds (VOCs) and particulate matter when the gas pathway is intend...

The biocompatibility systemic toxicity tests are in vivo systemic tests used to evaluate the impairment or activation of a system, rather than the impairment of individual cells or organs.

The Biocompatibility Subacute and Subchronic Toxicity test is used to evaluate the toxicity effects likely to arise from repeated exposures would have on a patient, including any compound toxicity effects.

Chemical Characterization is a powerful methodology for addressing biocompatibility endpoints, providing a risk assessment of biocompatibility using chemical, biocompatibility, and patient exposure data.