Expert knowledge and experience in federal CLIA regulations and California clinical and public health laboratory compliance requirements including personnel, QA, QC and nonFDA-approved test method validation for all specialties including genetics and molecular biology.  Experienced in onsite GLP evaluation, ISO, and/or data audits of national and international research laboratories and clinical trial sites.

Provide consultation services, document reviews, onsite audits, and personnel evaluations for new and existing clinical laboratories to assess readiness for state and/or CLIA inspections, and/or overall compliance with state and federal laboratory laws.

Laboratory Consulting Services, Inc.

Org chart

Teams

Offices