Sanket’s Laboratory medicine is an evidence-based medicine based on its testing on tissue, fluid, and/or other specimens to assist clinical staff and medical doctors in disease identification and further in providing patients with the optimal medical treatment. Sanket provides world class accuracy in chemical, cytological, haematological, histological, and pathological techniques in its work in acquiring diagnostic results.
Over 70% of the decisions of medical treatments in Zambia rely on diagnostic results from the medical laboratory which implies that Sanket’s laboratory medicine; which tested 1.5 million patients in 2021 and provided 7.5 million accurate tests has become the leading first-line health monitoring of the public in Zambia. Sanket’s quality control, EQA assurance and its world class management of more than 200 of Zambia’s leading technicians, laboratory scientists and medical clinicians along with the nation’s most advanced laboratory technologies ensure the high quality of public diagnostics in Zambia.
Accuracy and precision of the test results are the essential criteria for laboratory medicine, hence, systematic quality assurance is the cornerstone of clinical laboratory processing. There are two associated systems for medical laboratory accreditation that Sanket mimics in its NHIMA and HPCZ and other regulatory compliance which are the International standard system for medical laboratory, ISO15189:2012 offered by International Organization for Standardization; which provides international standards in medical laboratory and, the US system of lab accreditation through the College of American Pathologists (CAP accreditation) which is an accreditation programme based on ISO15189[6].
Sanket’s diagnostic testing (Analytical and Pro-Analytical Process) contains the best quality control because it is adherent to medical standardisation and quality management systems like ISO15189. Sanket follows the complete list of analytical variables that need to be monitored including sample labelling and registration, equipment and device performance, chemical validity, automated system performance, sample quality control, management of documentation for protocols, test reports, clinical reports, audit/quality assurance certificates and maintenance records, staff training and performance, environmental quality control etc. To rule out the warning and uncertainty, planning for a regular internal audit and EQA for quality assurance (e.g. once a month, with an annual external audit.