Biosafety Level You must comply with your country’s regulations. : {{entry.product.biosafetyLevel == -1 ? '-' : entry.product.biosafetyLevel}} Tariff Code: {{entry.product.euTariffCode}}
Biosafety Level You must comply with your country’s regulations. : {{entry.product.biosafetyLevel == -1 ? '-' : entry.product.biosafetyLevel}} Tariff Code: {{entry.product.euTariffCode}}
External Quality Assessment (EQA) designed for laboratories and clinics who are involved in the routine quantification of therapeutic drugs in serum
Test materials comprise human serum, urine, newborn calf serum, and human blood/plasma
TM rounds include: Antiepileptic drugs mixture, Cardiac drugs mixture, Analgesic mixture, Drugs for the treatment of substance related disorders 1 and 2, Psychoactive drugs, Smoking related drug, Immunosuppressive drugs
AT rounds include: Antibiotic drugs (these analytes are produced in collaboration with the UKNEQAS for antibiotics drugs)
Participants receive test materials at monthly and quarterly intervals
Performance of U.K. participants is reported to the National Quality Assurance Advisory Panel for Chemical Pathology and for Medical Microbiology