251 devices · GMDN 30503
These devices are designed to validate and calibrate immunoassays or other tests that detect multiple therapeutic drugs or drugs of abuse in clinical samples like blood, urine, or saliva. They ensure accuracy and reliability in laboratory testing by providing reference standards for comparison against patient specimens.
Control materials in this category are typically regulated as in vitro diagnostics (IVDs) and must meet performance standards for accuracy, precision, and traceability. They are often supplied as liquid or lyophilized formats, requiring proper storage and handling to maintain stability before use.
This category summary is AI-generated from the GMDN nomenclature and has not been verified by a human reviewer.