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Elvira Cawthon works with EAS clients on comprehensive clinical trial protocol development for medical device, IVD and device-drug combination product applications. With a focus on data efficacy, feasibility and usability she also provides ongoing study monitoring activities, outcomes analysis and report writing for FDA 513(g) submissions; FDA Q-Sub submissions, IDE submissions, and more. She has presented on FDA Presubs and IRB on behalf of EAS at FDLI’s intro to Device Law and authored articles in peer-reviewed journals.

Posted in Who’s Who at EAS.