UNSPSC 41151716: Clinical toxicology control material

In this classification, a Clinical toxicology control material is a device intended to measure Clinical toxicology control material for clinical toxicology purposes. US FDA regulates Clinical toxicology control material under 21 CFR 862.3280 and under FDA product code DIF

UNSPSC 41151716 Clinical toxicology control material is a Commodity code that sees virtually no recent state and local procurement activity aligned with its taxonomy definition. The single opportunity tagged to this code—a Harris County, Texas RFP for a unit dose packaging system posted September 4, 2026—bears no clear relationship to clinical toxicology control materials and lacks sufficient scope detail to confirm relevance. The source material provides no additional state or local solicitations for clinical toxicology reference standards, quality control specimens, calibration materials, or related laboratory reagents that would typically anchor purchasing under this code.

State and local laboratories, public health departments, and health-system procurement offices occasionally acquire toxicology reference materials and positive/negative control specimens for drug screening, forensic analysis, and clinical chemistry validation, but the recent-opportunities block shows no activity supporting that pattern. The code appears dormant in the current state and local contracting cycle, making it difficult to characterize active issuing bodies, geographic concentration, or representative procurement patterns. A business development professional should monitor for future activity but should not prioritize capacity building or pursuit strategy around this code without evidence of sustained opportunity volume.