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21 CFR Part 58 FDA GLP Services

QA Consulting and Testing, LLC is the industry leader in 21 CFR Part 58 of FDA Good Laboratory Practice for non-clinical laboratory studies. We have been assisting companies like yours with 21 CFR Part 58 needs for over a decade.

Trust our experience, industry knowledge, and GLP expertise. Call us today! (801) 372-7177


QA Consulting and Testing, LLC provides comprehensive 21 CFR Part 58 GLP (Good Laboratory Practice) and QA (Quality Assurance) services for non-clinical laboratory studies that include facility inspections, document review, comprehensive inspections and audits, study monitoring, training, and GLP laboratory program development.

Von Isaman, President of QA Consulting and Testing, LLC has served as the QA Administrator for a large number of industry studies at various locations, assuring GLP compliance. Von has extensive experience in:

  • Corporate laboratory SOP creation and analysis

  • Working with contract laboratories

  • Assisting medical device and pharmaceutical companies with 21 CFR Part 58 FDA GLP compliance

  • Reviewing protocol to ensure it complies with regulations

Give us a call today at: 801.372.7177

Test Tubes


PO Box 627
Salem, Utah 84653

(801) 372-7177

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