Marta Rivas

Marta Rivas has extensive experience in the medical device industry, currently serving as an Evaluatrice de dispositifs médicaux at GMED since September 2021. In addition, Marta has been the Directrice qualité et affaires réglementaires at H4D - Health for Development since 2012, overseeing regulatory affairs including CE marking, 510(k) submissions, global matériovigilance, and compliance with various regulatory bodies. Responsibilities include managing quality management systems, conducting audits, and preparing clinical evaluation reports. Earlier roles include Evaluateur dispositifs médicaux at ANSM and Consultante chef de projet dispositifs médicaux at Altran Engineering Solutions, where Marta led multiple projects for notable clients such as GE Healthcare and Renault Technocentre.