Webcasts

Webinar Date/Time: Tue, Mar 14, 2023 11:00 AM EDT

Webinar Date/Time: Tuesday, February 14th, 2023 at 10am EST|7am PST|3pm GMT|4pm CET

Webinar Date/Time: Thu, Jan 26, 2023 11:00 AM EST

Webinar Date/Time: Tuesday, January 24th, 2023 at 11am EST|8am PST|4pm GMT|5pm CET

Webinar Date/Time: Wed, Nov 30, 2022 10:00 AM EST

Webinar Date/Time: Tuesday, December 13, 2022 at 10am ET | 3pm GMT | 4pm CET

Webinar Date/Time: Tuesday December 6th, 2022 at 11am EST | 8am PST | 4pm GMT | 5pm CET

Webinar Date/Time: Tuesday, November 29th, 2022 at 11am EST|8am PST|4pm GMT|5pm CET

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.

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

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.

Thu, Oct 20, 2022 11:00 AM EDT Helping cancer centers rapidly and more accurately assess patient populations can dramatically reduce the time it takes cancer centers to gather the data to complete sponsor feasibility surveys, while increasing the specificity, clarity, and understanding of patient populations. Cancer centers can select trials with greater confidence of their ability to enroll patients and thereby reach targets for their research program without bias.

Wed, Oct 19, 2022 11:00 AM EDT In this webinar, Advanced Clinical will explore best practices for writing custom patient narratives and how this approach adds value for sponsors, site staff, patients and regulators.

Thursday, October 13, 2022 at 10 am EDT|7am PDT|3pm BST|4pm CEST

Wednesday, October 12, 2022 11am PDT | 2pm EDT | 7pm BST | 8pm CEST Real-world-data (RWD) leads to real-world results. Learn how RWD & patient tokenization are streamlining clinical trials and ensuring successful results.

Wed, Sep 21, 2022 11:00 AM EDT No site should have to turn down a clinical trial due to drug sourcing requirements; no clinical trial participant should have out-of-pocket expenses secondary to participating in a clinical trial; and no sponsor should have to incur expensive drug waste nor do extensive forecasting analyses – we know this, but it has happened. However, the next big thing is here to solve those issues and more, and you won’t want to miss this webinar with Myonex’s Tom Gregson, Samit Bhatt, and Todd Luckritz, discussing current trends and solutions to many clinical trial sponsor pain points with Mary Veazie, clinical research finance leader with 20+ years' experience.

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.

Tue, Sep 13, 2022 11:00 AM EDT Reduce clinical monitoring costs by deploying a risk-based strategy. Learn how technology and analytics enable actionable insights, reduce trial costs and improve patient safety and data quality.

Wed, Sep 7, 2022 11:00am EST | 8:00am PST | 4pm BST | 5:00pm CEST Decentralized Clinical Trials (DCT) is one of the hottest buzzwords in Life Sciences and Connected Health organizations today. Like any new approach, challenges and roadblocks are common and knowing how to solve for them will empower your organization to accelerate your trial deployment, speeding return of results and time to market.

This webcast is now on demand. Real-world data networks are changing how data is collected and leveraged for evidence generation. A tech-enabled platform approach can significantly automate and reduce the burden of clinical study programs and registries, improve site and patient engagement and lower costs.

Wed, Jul 27, 2022 10:00 AM SGT (Tue, Jul 26, 2022 10:00 PM EDT) Join this webinar to learn how JAPAC IQVIA Biotech leverages data and expertise to support your strategic drug development for early oncology assets to ensure your success.

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.

Available On Demand The use of real-world data in clinical research is on the rise – but what are the logistics of tokenizing and linking RCT data? Parexel and Datavant discuss how to implement tokenization within a clinical trial in an informative webinar. Tune in to learn more!

Wednesday, July, 13th, 2022 at 11am EDT | 10am CDT | 8am PDT It’s no secret that hybrid and decentralized trials (DCT) are here to stay. Yet despite adoption, questions, myths, & rumors about what it means to “decentralize a trial,” persist. Find out the truth from Medable.

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.

Now Available On Demand! Learn best practices to optimize your clinical supply chain management to decrease costs, improve productivity, and increase patient retention for a more successful clinical trial.

Thursday, May 26, 2022 at 11am EDT 1. Learn of a new integrated monitoring approach to speed your trials, improve study quality while mitigating risks 2. Understand how integrated monitoring solutions are using innovative technology and analytics to streamline and automate processes

Tuesday, May 24th, 2022 at 1pm EDT|10 am PDT|6pm BST|7pm CEST Simply handing off multi-million-dollar studies to CROs without carefully crafted plans for communications and reporting operational data as the study unfolds is hardly a wise move, yet what kind of oversight is needed? Technologies that track how studies unfold are essential but putting that information to good use requires turning real-time visibility into actionable data.

Thursday, May 12, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Many organizations have yet to figure out how to fit digital, hybrid, and decentralized clinical trial methods into their existing ecosystems in a scalable and efficient way. This webinar will go through the complexities that decentralized and hybrid methodologies bring to first-generation platforms, and how a single, unified platform enables interoperability and flexibility to help truly unlock the potential of these digital study methods.

Now available on demand! Optimizing clinical development plans requires trade-offs across competing factors. Join us for an expert panel discussion exploring how coupling innovative development strategies with analytical tools can drive better drug development decisions.