04.22.24 -- Enhancing Clinical Trial Compliance And Efficiency

Join the movement to increase clinical research site capacity. IQVIA One Home for Sites serves as a neutral aggregator, connector, and communicator of the key systems and tasks sites need to perform.

Watch James Stringer's presentation from the October 2023 Clinical Leader Solutions Expo: IRT Showcase to learn how site burden can be reduced by having more consolidated platforms.

Our self-service or full-service model, modular, off-the-shelf Interactive Responsive Technology (IRT) system offers you a customized experience without the custom price tag.

Participation visits can impose an extra strain on patients. To gain insight from the perspective of clinical sites, see what this clinician had to say regarding their experience with Greenphire.

Learn how this distinctive approach centered on enabling clinical trial sponsors to gather data and generate evidence ensures the successful acquisition of diverse information.

By addressing the unique hurdles tied to regulations in European clinical trials, eBinders offer a streamlined approach to managing electronic trial documentation.

In this episode on pediatric clinical trial challenges, industry experts provide insight into their experiences and recommendations on decentralized clinical trial features for pediatric research.

Delve into this use case where Citeline’s Real-World Data was used to inform clinical development strategy and differentiate target product profiles through patient journey mapping.

With expanded access to a wider range of demographics and billions of additional Mx and prescription Rx encounters, discover how Pulse can optimize the pool of potential trial participants.

Discover how this EHR-to-EDC integration platform streamlines data entry efforts at clinical trial sites, simplifying and accelerating the transfer of source data.

Part of the elluminate Clinical Data Cloud, elluminate RBQM provides a centralized platform for data sources to enable a more focused, data-driven risk assessment for oversight and compliance.

The clinical trial process requires effective collaboration and exchange of critical documents between sponsors and sites. See how SIP goes above and beyond to overcome these challenges.