Webcasts

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.

Transforming Site Solutions: How Intelligent Technology Reduces Pain Points in Clinical Research  

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.




Are Your Patient Narratives Too Broad? 

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


Demystifying AI/ML for Data Management

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.  

The Key to Clinical Trial Success: Patient Tokenization

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.

Happy Sites, Happy Patients & Happy Sponsors: Eliminate the Site Burden of Drug Sourcing While Improving Patient Recruitment

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.

eConsent for complex clinical trials

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.

Transforming Data Into Insights and Outcomes in Risk Based Quality Management (RBQM)

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.

The Problem with Decentralized Clinical Trials and How to Solve for Success

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.

Real-World Data Networks: Automating & Reducing the Burden of Clinical Studies and Registries

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. 