CovarsaDx
Tania Vogel is a seasoned regulatory affairs and quality strategist currently serving as a Sr. Regulatory Affairs & Quality Strategist at CovarsaDx, where responsibilities include developing and implementing regulatory and quality strategies to ensure compliance with international standards. Previous experience includes a role as Sr. Quality Consultant at Fang Consulting, focusing on harmonizing regulatory affairs procedures for multiple business units, and positions in quality control and microbiology at Lifecore Biomedical, Brandless, Inc., and the FDA, where analytical and compliance expertise was demonstrated. Tania holds a BS in Interdisciplinary Science from South Dakota Mines and a BS in Criminal Justice from Colorado Technical University.
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CovarsaDx
We do IVD and Medical device trials differently, because these studies are exclusively what we do. Any CRO can execute a protocol, and some claim to have a “Department” dedicated to IVD and Medical Devices. With CovarsaDx, clients experience the unparalleled advantages of clinical studies with a boutique CRO where every advisor is an industry specialist in IVD and Medical Device trials, and each has the experience to engage clients in the strategic planning and successful execution that brings clinical studies to the finish line on time. Clients benefit from: Customized study strategy and strategic design Full support of an extensive network of clinical sites and leading principal investigators The agility to rapidly adapt to changing design needs and the fluid regulatory environment CovarsaDx is an independent CRO that prioritizes regulatory deliverables and client needs backed by trusted, proven clinical research experience and resources. Get to reliable, powerful clinical truth with CovarsaDx.