Establishing Molecular Testing in Clinical Laboratory Environments, 1st Edition

This guideline provides comprehensive guidance for planning and implementation of molecular diagnostic testing, including strategic planning, regulatory requirements, implementation, quality management, and special considerations for the subspecialties of molecular genetics, infectious diseases, oncology, and pharmacogenetics. 

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Publication Details

Chairholder: Leslie Hall, MMSc, M(ASCP) and Jean Amos Wilson, PhD, FACMG, CGMB

Date of Publication: November 30, 2011

ISBN Number: 1-56238-773-1

Order Code PDF: MM19AE

Order Code Print: MM19A

Edition: First

Pages: 252

MM19 Additional Details

This archived document is no longer being reviewed through the CLSI Consensus Document Development Process. However, this document is technically valid of as March 2017. Because of its value to the laboratory community, it is being retained in CLSI’s library.