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Wouter joined IQVIA in September 2019 from the ‘genae’ acquisition, where he was part of the senior management team for almost 10 years – first as Director Clinical Research and then as COO. Before this he spent over 15 years in the medical device arena working in a variety of roles on both the investigator […]
How effective and early medical device strategy development can optimize your design and development process Written By: Marianna Gofman, Senior Consultant, IQVIA MedTech Regulatory Solutions Europe While continuous innovation supports new product design and development, it’s no wonder the healthcare industry is pressuring medical device companies to increase safety and efficiency, while also being innovative […]
Victoria Cavendish, Ph.D. leads the IQVIA MedTech Regulatory Solutions team. She joined IQVIA in 2016 and is responsible for strategy execution, including customer engagement and service delivery. Victoria has over 20 years of experience in supporting medical device and diagnostics companies navigate the regulatory, quality and clinical evidence landscape. Give us IQVIA’s elevator pitch. IQVIA […]
Regulators’ Growing Adoption of Real World Evidence Brinda Sriskantha, PhD, Director, Real World Solutions, IQVIA MedTech and Michelle Bulliard, Vice President, Real World Solutions, IQVIA MedTech Regulators have been steadily increasing their use of real world evidence (RWE) to support decision-making. Simultaneously, access to real world data (RWD) continues to increase, and there’s growing clarity […]