Seronorm™ Immunoprotein Liq

Serum Indices Quality Control materials for clinical laboratories to monitor and validate analyzer performance across hemolysis, lipemia, and icterus parameters. Ensures accuracy and reliability of patient diagnostic results on automated chemistry and hematology systems worldwide.

Human control sera for quality assurance and validation in clinical laboratory testing. These reference materials enable standardization and verification of diagnostic assays across hematology, immunology, and chemistry analyzers. Customizable formulations support method validation and regulatory compliance in in vitro diagnostic workflows.

Human control sera for in vitro diagnostics calibration and quality assurance. Provides reference materials for validation of diagnostic assays and laboratory test methods. Produced to specified standards for clinical chemistry and immunodiagnostic applications.

External quality control material for clinical laboratories enabling periodic multi-sample distribution and real-time result monitoring across laboratory networks. SEROQAS supports multiple analytes including NT-proBNP, CK-MB, hsTnI, AMH, and CRP with compatibility across all major analyzer platforms and POCT devices.

Normal human serum calibrators and controls for immunoassay standardization and performance validation.

Proficiency testing materials for serum chemistry analytes including electrolytes, metabolic markers, and proteins. Enables laboratories to monitor accuracy and precision of chemistry analyzers through external quality assessment programs.

Internal quality control material for clinical laboratory analyzers supporting immunology and clinical chemistry testing. Designed for multiple biomarkers including NT-proBNP, CK-MB, hsTnI, and CRP with up to 3-year shelf life. Compatible with all major laboratory systems and POCT devices to ensure diagnostic accuracy and precision.

Serum control material for bone marker assays used in clinical laboratories to validate test accuracy and ensure reliable patient results. Designed for quality control in bone metabolism testing across automated diagnostic platforms. Enables laboratories to maintain consistent performance standards and meet regulatory compliance requirements.

High-purity protein conjugates and reference standards for development and validation of clinical immunoassay diagnostic platforms.

Albumin is a diagnostic reagent used in clinical laboratory testing and in vitro diagnostics. This product supports various immunoassay and serological applications in hospital and laboratory settings. It functions as a key component in diagnostic test formulations and quality control procedures.

Reference materials and quality controls for in vitro diagnostics and clinical genomics applications. These biological and reagent components enable laboratories to validate assay performance, ensure result reliability, and participate in proficiency testing and external quality assessment programs across diagnostic testing workflows.