Increasingly, regulatory authorities are seeing the value of real world evidence (RWE) to evaluate a product’s safety and effectiveness. This changing environment presents you with new opportunities to increase the effectiveness and efficiency of your safety and regulatory studies.
At IQVIA, our global scientific and operational experts are developing innovative approaches for RWE study design and execution. Leverage secondary and primary data directly from patients and physicians to plan the most efficient study design for your needs. Applications include
To best support your research, IQVIA nurtures extensive scientific affiliations and maintains a strong commitment to research excellence. We are active partners and participants with OMOP, ENCePP, EUnetHTA, IMI, the Department of Health and Human Services, and maintain numerous academic affiliations. We help you meet regulatory needs, using RWE to accelerate approvals and label expansions in the U.S. and EU.