CovarsaDx
Marisa Meeks currently holds the position of Senior Quality Associate and Technical Writer at CovarsaDx, starting in March 2023. Prior to this role, Marisa served as a Quality Specialist at Hycor Biomedical LLC from January 2017 to March 2023, where responsibilities included conducting internal quality audits and managing supplier control within the Quality Management System. Marisa's experience also encompasses a temporary position as a Quality Specialist at Hycor Biomedical from April 2010 to February 2011, focusing on document auditing and procedure development. Marisa dedicated five years as a full-time stay-at-home mom from September 2005 to August 2010. Earlier career experience includes serving as Associate Director of Regulatory Compliance at Diagnostic Products Corporation from May 1998 to June 2003. Marisa Meeks earned a Bachelor of Arts in Biological Sciences from California State University, Fullerton between 1985 and 1992.
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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.