IQVIA

Articles by IQVIA

Optimized Clinical Trials: A “From the Field” Webinar

Webcasts

Part 1: Wednesday, November 2nd, 2022 at 9am EDT|6am PDT|1pm GMT|2pm CET Part 2: Wednesday, November 16th, 2022 at 9am EST|6am PST|2pm GMT|3pm CET As the pandemic caused sponsors to implement new delivery models faster than originally intended, IQVIA embraced this challenge with innovative approaches that enable sponsors to achieve a new level of patient engagement without compromising the trial process. Join our panel of experts as they share case studies on how IQVIA has partnered with sponsors and sites to tackle recruitment and retention, leveraging patient data and technology to drive better engagement through innovative experiences and processes.

Using IRT Data to Automate and Optimize Clinical Supply

Webcasts

Wednesday, November 9th, 2022 Session 1: 2pm CET|1pm GMT|8am EST Session 2: 11am EST|8am PST|4pm GMT|5pm CET Discover how Cenduit IRT’s industry partners have reduced waste and cost during their trial by applying automated drug supply optimization tools

Turn Real-World Data Insights Into a Personalized Trial Journey for Every Patient

Webcasts

Part 1: Wednesday, November 2nd, 2022 at 9am EDT|6am PDT|1pm GMT|2pm CET Part 2: Wednesday, November 16th, 2022 at 9am EST|6am PST|2pm GMT|3pm CET We’ve grown as an industry; clinical research and drug-to-market development has been on the forefront of the optimizations towards breakthrough innovations and treatments. Learn strategies incorporating real world data and technology to help optimize the clinical trial journey in a way that meets the patient where they live.

eConsent for complex clinical trials

Webcast

Tuesday, September 20, 2022 at 9am EDT | 6am PDT | 2pm BST | 3pm CEST As clinical trial protocols become more complex, patient informed consent forms and processes become more complicated as well. In this webinar, IQVIA Complete Consent leaders will share how a robust eConsent solution can be customized to support these complex multi-stage studies and high-risk patient populations with an efficient customized, site- and participant-friendly consenting experience.

Ensuring Data Quality in a Complex Trial Landscape

Webcast

Tue, Jul 26, 2022 11:00 AM EDT Register for this free webinar to learn about a new data analytics platform enabling you to ingest, normalize and use data from the vast variety of clinical data sources and drive faster, deeper data actionable insights to improve study quality for better outcomes.

Case Study: Building integrations that reduce site and sponsor burden and improve the patient journey

Webcast

Thursday, June 9, 2022 at 11am EDT The right technology integrations can simplify sponsor and site effort while improving the ability to make decisions during clinical studies. Learn how one vendor/sponsor collaboration produced an IRT eCOA integration that improved data quality and usability, drove new efficiencies for sites and sponsors while optimizing study delivery, management and change management.