External Quality Control - SEROQAS

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.

Quality control materials, pooled specimens, and reference standards for in vitro diagnostic assay development and validation. Supports internal and external quality control, proficiency testing, and biomarker research using standardized human blood products and tissue samples in frozen, fresh, or lyophilized formats.

Pre-formulated quality control materials in blood and serum matrices for clinical laboratory testing. Includes 200+ analytes spanning therapeutic drug monitoring, endocrinology, and trace element testing. Provides audit-ready documentation and stability data without in-house manufacturing.

Manufactured quality control specimens used to verify the accuracy and reliability of diagnostic laboratory instruments and assays. These materials ensure consistent performance and compliance with clinical laboratory standards.

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.

Fortress Diagnostics' quality control range Seraqual is utilised in laboratories across the world to enable laboratories to confidently produce accurate results.

Seronorm™ CRP Liquid is an independent third-party quality control material for C-reactive protein testing in clinical laboratories. It enables day-to-day and inter-laboratory result comparison across different analytical methods and instruments. Designed to match patient sample behavior and comply with ISO 15189 standards for reliable diagnostic quality assurance.

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.

Rigorous QC protocols for gold conjugates, antibodies, and diagnostic reagents ensuring sensitivity and specificity. Batch-consistent testing supports regulatory submissions.

Multiple composite quality control materials with high-quality reputation that provide reliable performance evaluation for laboratory experiments. These products ensure consistent and accurate testing results.

Comprehensive quality control platform for validating diagnostic test performance and laboratory compliance. Includes tools for internal quality checks, external proficiency testing, and regulatory documentation.