Manufacturers of in-vitro diagnostics must regularly check their medical test kits and validate the results obtained.
For this purpose, so-called validation panels are absolutely necessary, with which important analysis parameters such as LOD (limit of detection) or LOQ (limit of quantification) can be determined and checked.

In the field of hepatitis C diagnostics, BIOMEX now offers a range of new validation and seroconversion samples that can be used to advance product development and ensure compliance with quality standards.

More information about available HCV panels can be found here.