Webcasts

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.   

Ensuring Data Quality in a Complex Trial Landscape

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.

Is Oversight a Burden or Pivotal to Operational Efficiency?

Tuesday, April 26, 2022 at 11:00 EST
Today’s Data Managers are presented with the challenge of ever-increasing data volumes, evolving data collection devices, clinical trial conduct strategies and industry pressures. They need to deliver this against the need for ever faster drug development, while maintaining the highest quality and without increasing cost. IQVIA will share their Intelligent Data Cleaning strategy leveraging centralized data flow and issue management, digitized workflow and end-to-end standards to drive automation that allows the data manager and the study team to transform their interactions with the data and process.

Centralized Data Flow and Connected Workflow Intelligence to Enable Data Science in Clinical Trials: A day in the life of an IQVIA Data Manager

Tuesday, March 22, 2022 at 11am EST
In this webinar, IQVIA eCOA leaders Anthony Mikulaschek, Melissa Mooney and J.C. Wilson will explore how to implement a bring your own device (BYOD) strategy within your study, relevant BYOD regulatory considerations, and where the market is going from here. Specific points within this webinar include how the pandemic has furthered the adoption of BYOD, the benefits of BYOD, including reduced patient burden, reduced costs, and increased patient compliance, and how to develop a BYOD strategy and considerations to be made during planning and implementation. 

BYOD is Here to Stay: Considerations for implementing a BYOD eCOA strategy

Wednesday, March 9, 2022 at 11am EDT
Are you looking for a digital approach to protocol training? See the cross-trial solution that’s eliminating repetitive trainings and saving precious time during study start-up, all while boosting quality and auditability.  

Elevating the Site-Sponsor Experience: Learning Management SaaS in Clinical Trials

Thursday, 24th February 2022, 11:00 EST** Data plays a central role within drug discovery and as decentralized trials become more prevalent in the industry, the need to process and engage with enterprise level solutions and the integration of technology to map data to standards become a must. 

As a central conduit to this IQVIA Biostatistics will share the importance of how to maximize end to end efficiencies through compliance to standards and together provide an understanding to how data flow is an integral part of transformative biostatistics technologies and processes can accelerate clinical development across an organization through an innovative outsourcing approach.  

Clinical Data Flow: The Foundation of a Biostatistics Ecosystem within a Data Universe 

*** Thursday, June 17, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Join this webinar to hear best practices on how to enhance site-sponsor collaboration, compound efficiencies and accelerate trials by enabling end-to-end document exchange between sponsor eTMF systems and Florence’s leading eISF solution through Cognizant SIP.    ***On demand available after final airing until June 17, 2022***

Creating an Integrated Digital Pathway for Sites and Sponsors

*** Friday, June 11, 2021 at 11am EDT *** Data plays a central role within drug discovery and as decentralized trials become more prevalent in the industry, the need to process and engage with enterprise level solutions and the integration of technology to map data to standards become a must. 

As the central conduit to this IQVIA data management will share the importance of how systemic compliance to standards together with a central data strategy can accelerate clinical development across an organization through an innovative FSP approach.***On demand available after final airing until June 11, 2022***

Connected Data Flow and Standards: A data management approach combining standards, technology and data flow to accelerate FSP clinical development

*** Wednesday, May 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** It has never been more important for sponsors, monitors, and sites to learn how best to conduct monitoring visits remotely and securely. Learn about implementing remote monitoring, including analyzing implementation challenges, understanding the FDA’s guidance on delayed monitoring, and more.   ***On demand available after final airing until May 26, 2022***

Remote Monitoring: Study Compliance in a Changing World

*** Monday, May 24, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Most organizations deal with the vulnerabilities that exclusive point solutions create. Join industry leaders Oracle and IQVIA to understand how inclusivity and a flexible environment can help you employ new approaches faster, and the benefits of collaboration in today’s clinical trials ecosystem.*** On demand available after final airing until May 24, 2022 ***

Webcasts: Data Management