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Mainz Biomed: Karen Richards

Mainz Biomed has appointed Karen Richards as VP of regulatory affairs. She will also serve as SVP of in vitro diagnostics and quality at Precision for Medicine. According to Mainz Biomed, Richards was responsible for the approval of laboratory tests in all 50 states in the US requiring a license and has implemented quality systems for diagnostic products to meet various regulatory and certification requirements, including those of the US Food and Drug Administration, CLIA, and the College of American Pathologists.