Fact Sheet
How the Rapidly Evolving Regulatory Landscape Will Drive the Increasing Need for Post-market Safety Studies
How to demonstrate real-world safety, performance, and effectiveness with post-market safety studies
Oct 26, 2021
Download

As a proven MedTech partner with trusted expertise, we help our customers generate the right real world evidence (RWE) to meet stakeholder needs with confidence. Post-market surveillance is a crucial process to ensure that medical devices continue to be safe and effective. Learn how IQVIA can support you with post-market safety studies through our high quality delivery excellence, innovative approaches, and reliable regulatory expertise.

Contact Us