Therapeutic Drug Monitoring (TDM) Quality Assessment Materials

A comprehensive laboratory solution for therapeutic drug monitoring applications, enabling clinicians to measure and manage drug levels in patient specimens.

Therapeutic Drug Monitoring (TDM) solutions for LC-MS/MS analysis, including calibrators and quality controls in human matrix. Enables standardized clinical measurement of drug levels to optimize dosing and patient outcomes across laboratory networks.

External quality assessment materials used by laboratories to evaluate testing accuracy and competency. These specimens enable participation in proficiency testing programs required for laboratory accreditation.

A comprehensive laboratory solution for therapeutic drug monitoring in clinical settings. This system enables accurate measurement and management of drug levels in patients.

A biological drug monitoring system that measures therapeutic drug levels in patient samples. The system supports clinical decision-making through automated analysis of medication concentrations.

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.

Quality control materials for clinical laboratory analyzers supporting diabetes and metabolic testing. Designed for internal and external quality assurance across multiple analyte parameters with up to 3-year shelf stability. Compatible with all major laboratory instrument platforms including POCT devices.

Quality control material for high-sensitivity troponin I testing in cardiac diagnostics. Compatible with POCT and laboratory analyzer systems for consistent measurement performance.

A point-of-care platform for continuous monitoring of drugs with narrow therapeutic windows including propofol and lithium. The system enables informed medical decision making through real-time drug level measurement.

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.

Internal quality control materials for clinical laboratory analyzers with up to 3-year shelf life. DIQAS supports real-time monitoring of test results across global laboratories and enables performance comparison for continuous quality improvement.

Quality control materials for monitoring precision and reproducibility of anti-müllerian hormone (AMH) testing methods in serum, plasma, and other specimens. Ensures accuracy of reproductive health diagnostics.