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.
Member pricing between $42.00 and $119.00Nonmember Price: $140.00
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
MM19 Additional Details
This document is no longer being reviewed as part of our consensus process. However, because of its usefulness to a limited segment of the healthcare community, we are continuing to make the document available for its informational content.