CLSI Blog Articles
Read the latest articles about CLSI and laboratory standards in the official CLSI Blog. Browse our most recent blog articles below.
While laboratory workers are always vigilant against laboratory-acquired infections, uncertainty has arisen in the medical laboratory community about the most effective way to protect against COVID-19. The United States Department of Labor Occupational Safety and Health Administration (OSHA) provides guidelines for safe COVID-19 specimen processing, as well as information about proper personal protective equipment (PPE) for laboratory workers.
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The bipartisan bill, Verifying Accurate Leading-edge IVCT Development Act (VALID), was introduced to Congress on March 5, 2020. This legislative effort, if enacted, will overhaul the regulatory oversight of in vitro diagnostics (IVDs) in the United States and create a single system for regulation of LDTs and manufacturers’ IVCTs.
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Taking blood samples from children can be difficult for the phlebotomist. Ensuring safety while accounting for a pediatric patient’s emotional and physical well-being is of the utmost importance.
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Measurement procedure comparison is one of the most common techniques used by both manufacturers and medical laboratorians to estimate the bias of an in vitro diagnostic (IVD) measurement procedure relative to a comparator.
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At the invitation of US Centers for Disease Control (CDC), CLSI’s Global Health Partnerships (GHP) visited Tanzania, one of the first countries with which GHP partnered, in 2005. This was to be the first of many visits and a long-term partnership.
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Interference screening in clinical chemistry is conducted by paired-difference testing: samples with and without the interferent are measured, and the measurand concentration difference is determined.
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M24 is an important foundation guideline that supports CLSI’s library of antimicrobial and antifungal susceptibility testing documents.
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On February 26 and 27, 2020, CLSI will host its annual M100 updates webinar.
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CLSI’s GHP team will be hosting a workshop on February 9-11th at the Medlab Middle East exhibition in Dubai. Participants will learn how a laboratory can establish an internal audit program to enhance the quality of its services through continual improvement.
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EP35—Assessment of Equivalence or Suitability of Specimen Types for Medical Laboratory Measurement Procedures, 1st Edition provides recommendations for assessing clinically equivalent performance for additional specimen types.
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