About me
I am passionate about innovation, emerging technologies, and artificial intelligence, with a strong belief in the critical importance of quality systems in managing the lifecycle of medical products.
With 10 years of experience in quality system management, clinical evaluation, technical documentation development, auditing, and certification of medical and in-vitro diagnostic products, I co-founded A3Z Advanced in 2016, a boutique consulting firm that provides comprehensive support to manufacturers of medical and in-vitro diagnostic products. From product conception to post-marketing support, we offer expert guidance on transitioning to MDR and IVDR for mass-produced and hospital-based products, ensuring regulatory compliance and maximum customer satisfaction at every stage of product development.
With 20 years of experience in analytical science and managing GLP-compliant bioanalytical laboratories for preclinical, clinical, and scientific research, I am dedicated to ensuring that laboratory operations meet the highest standards of quality, regulation, and operational efficiency.
Additionally, I am honored to participate as a professor in several master's programs and industry training courses, sharing my knowledge and experience with the next generation of professionals.
