Updated on 18 October 2013
The objective of Clinical Laboratory Improvement Amendments (CLIA) certification is to ensure the accuracy, reliability and timeliness of test results regardless of where the test is performed
Singapore: WuXi PharmaTech, a leading pharmaceutical, biotechnology and medical device R&D outsourcing company with operations in China and the US, has cleared the survey by Centers for Medicare and Medicaid Services of the US Department of Health and Human Services relating to CLIA (Clinical Laboratory Improvement Amendments) standards, thereby receiving CLIA certification for its genomics clinical laboratory.
CLIA standards, established by the US Congress in 1988, relate to all clinical laboratory testing on specimens derived from humans in the US to give information for the assessment, diagnosis, prevention, and treatment of disease or other impairment of health.
The objective of CLIA is to ensure the accuracy, reliability and timeliness of test results regardless of where the test is performed. Receipt of a CLIA certificate allows WuXi's genomics laboratory to undertake certain clinical trial gene sequencing projects.
"We are excited about the addition of CLIA-certified clinical laboratory testing to our suite of service offerings," said Dr Ge Li, CEO, WuXi AppTec. "WuXi is dedicated to the highest operational and quality standards. Our CLIA certification is an important milestone in realizing our vision to build an open-access technology and capability platform that enables anyone and any company to discover and develop therapeutic products to benefit patients."