Maria Fernanda Herrasti Campos
Maria Fernanda Herrasti Campos is a regulatory professional with experience in medical device validation, clinical technical support, and quality management within hospital and laboratory environments.
About Maria Fernanda Herrasti Campos
She specializes in regulatory documentation preparation, medical device validation, and compliance with Mexican and international frameworks, including COFEPRIS requirements, ISO 13485, MDR, FDA, and NOM-24. In her role at Pure Global, she supports regulatory submission projects in Mexico, coordinating timelines, managing client communication, and ensuring that technical documentation meets applicable regulatory requirements.
Prior to joining Pure Global, Maria worked in medical device distribution and healthcare solutions. She holds a bachelor’s degree in biotechnology from Universidad Anáhuac México.