Unlock the secrets to successful IVDR CE-mark submissions in our exclusive webinar, "Ask The Expert: IVDR - Early Experience and Feedback." This webinar is your key to understanding the ins and outs of the In Vitro Diagnostic Regulation (IVDR) and gathering valuable insights from seasoned professionals who have braved the early stages of this transformative regulation.
Whether you are a manufacturer striving to achieve IVDR CE-mark for your important diagnostic devices or an individual with a vested interest in the diagnostic device industry, our "Ask The Expert: IVDR - Early Experience and Feedback Webinar" is your gateway to knowledge, real-world experiences, and valuable connections.
Speaker Sarah Chavez, PhD
Dr.Sarah Chavez has worked on medical and regulatory writing for three years and has a BS in Biochemistry and a PhD in Molecular and Cellular Biology, with 25 years of laboratory bench experience. She has a strong understanding of a wide range of laboratory techniques, and has taught Genetics, General Biology, Cancer Immunology, and Global Health at the University level for the past 15 years. Prior to joining Criterion Edge, Sarah had extensive scientific writing experience in an academic environment, having written many large institutional research grants, regulatory documents, clinical trials protocols, book chapters, and manuscripts, as well as textbook chapters and educational materials for several large textbook publishers. Sarah’s strong background in basic research and her extensive experience with regulatory writing will allow her to assist companies with IVDR readiness as part of the Criterion Edge team.
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