Patient Associations
Impact the development of new therapies
IQVIA is helping the world’s leading patient advocacy associations in their efforts to accelerate the development of new treatments and elevate the quality of patient care.
IQVIA is helping the world’s leading patient advocacy associations in their efforts to accelerate the development of new treatments and elevate the quality of patient care.
Access IQVIA's industry-leading technology and full range of services, from strategic consulting and program design, to technology support and quality assurance. Our registry solutions can be designed to meet the needs of your members, and support both practice improvement and the promotion of research:
IQVIA's experts have extensive experience designing and deploying registries for some of the most prominent patient associations and medical specialty societies.
Interactions between patient organizations and life sciences companies.
Evidence-based research and dissemination of findings remain a key foundation to advance our collective understanding and interpretation of events, and to take actions that will shape the future for all stakeholders. This annual trend report is intended to contribute to that understanding.
Accelerating advocacy-led research and data initiatives
To accelerate and expand the impact of effective treatments, industry leaders must place emphasis on patients' needs. The key to driving change is the advancements in patient-centered registry technology that captures longitudinal information.
IQVIA's Patient Engagement framework supports comprehensive and consistent assessment and planning for the inclusion of patient needs and preferences
MSSs are often the best candidates to lead specialty-centric data standardization efforts because of their access to deep clinical expertise, physician-centricity, and strong convening power.
This white paper examines how registries can provide a valuable foundation for multi-arm, multi-company trials by fostering long-term, collaborative relationships between rare disease stakeholders and improving our understanding of diseases and treatment outcomes.