Introduction
According to FDA (2012), the CLIA are Federal government regulatory standards that ensure scientific and technical counsel to clinical laboratories in order for them to provide quality and best practices in clinical laboratory services. Clinical Laboratory Improvement Amendments is a combination of a chronology of events that have culminated to the current laws and regulations that guide the practice in clinical laboratories. The services offered by clinical laboratories are of critical importance in medicine and healthcare because they aid in monitoring diseases, including the pathophysiology of such diseases. Consequently, this contributes to the improvement of the quality of patient Continue reading...