Tuesday, November 2, 2021 at 11am EDT Get treatments to patients faster and deliver a better experience for both patients and clinical trial sites. Join IQVIA leaders Jeff Noll and Sara Pawley and learn how IQVIA matches the right connected device for each study protocol to enhance data quality, speed data collection, and accelerate trial outcomes.
Thursday, October 14, 2021 at 11am EDT. IQVIA eCOA leaders Kris Gustafson, Anthony Mikulaschek and Melissa Mooney explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what steps you should take to implement an eCOA in your next study. Specific points will include how to maximize efficiencies in eCOA deployments, gather real-time insights, and define an implementation strategy.
If you are responsible for delivering clinical or decentralized trials as a project lead, heading up clinical operations, medical or clinical monitoring, or driving your outsourcing strategy, attend this webinar to better understand the breadth of your choices. Monday, September 27, 2021 at 11am EDT
Tuesday, July 20, 2021 at 11am EDT It’s not often that a sponsor calls a clinical trial solution “life-changing,” but that’s how Bayer is describing the impact of IQVIA Clinical Trial Payments as the solution rolls out to more than 20 countries. Learn how it’s possible to pay sites 2-3 times faster, eliminate end-of-study reconciliation, and reduce time spent supporting payment processes by up to 90%.
Wednesday, July 14, 2021 at 11am EDT Looking for tested strategies to design and deliver truly patient-centric clinical trials? Join IQVIA experts for an insightful webinar on “Patient Centricity by Design: Improving patient engagement and retention while reducing burden with fit-for-purpose technology,” where you’ll hear how to enhance recruitment, strengthen patient and site relationships and deliver faster access through intelligent connections and decentralized trials approaches.
*** 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***
*** Wednesday, May 19, 2021 at 12pm EDT *** Join partners IQVIA Technologies and Salesforce for this webinar where we explore a new paradigm in life sciences where virtualization of clinical trials, both for patients and sites, has become a reality, and why it has become the industry’s new technological imperative. ***On demand available after final airing until May 19, 2022***
*** Wednesday, May 4, 2021 at 11am EDT *** Driving faster site activation for any clinical trial requires close interactions with sponsors to seamlessly execute a breadth of requirements to stay compliant while delivering to new levels of efficiencies ***On demand available after final airing until May 4, 2022***
*** Wednesday, April 28, 2021 at 11am EDT *** After a decade of dabbling with eConsent, it’s time for sponsors and technology providers to meet the demand to bring clinical trials directly to the patient at a global scale. Join this webinar to learn how to overcome the persistent challenges in eConsent adoption and deliver the promise of decentralized trials. ***On demand available after final airing until Apr. 28, 2022***
*** Monday, April 5, 2021 at 11am EDT *** Risk-based monitoring (RBM) continues to evolve and adapt to industry needs. Understand how innovative technologies and methodologies are driving new levels of study quality and changing clinical monitoring and how artificial intelligence, machine learning, predictive and advanced analytics are improving patient safety and overall study quality and operational efficiencies. ***On demand available after final airing until Apr. 5, 2022***
*** Thursday, November 19, 2020 | 4:00 pm-5:00 pm EST ***Japan, the second largest market for branded pharmaceuticals and innovation, is driven in part by Oncology with recent advances in genomic analysis technology. In addition, the Japanese market is driven by ongoing regulatory and government initiatives that reward innovation, shifts in population demographics, and increased disease awareness, and identifiable patient populations, amongst other factors. ***On demand available after final airing until Nov. 19, 2021***
***Live: Thursday November 12, 2020 at 11am EST***Oncology trials of various types and phases present unique challenges for effectively conducting trials, and firms are implementing risk-based monitoring (RBM) practices to improve quality and patient safety.***On demand available after final airing until Nov. 12, 2021***
Learn more about global regulatory acceptance of real-world evidence in a regulatory submission. Understand how to identify opportunities to incorporate real-world Evidence in your submission package. Live: Tuesday, Apr. 7, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 7, 2021. Register free
Enter a new era of clinical development planning. Use the power of “big data” and machine learning to generate more accurate plans that embrace uncertainty. Learn how to improve your development planning strategy while reducing trial costs and durations. Live: Thursday, Jan. 30, 2020 at 11am EST | 10am PST | 4pm GMT | 5pm CET On demand available after airing until Jan. 30, 2021. Register free
Regulatory requirements continually change, requiring the use of new innovative approaches, including technology advancement and process automation. Join us and take advantage of lessons learned from your peers to eliminate bottlenecks and leverage up-to-date regulatory intelligence to mitigate risks. Live: Tuesday, Dec. 10, 2019 at 11am EST On demand available after airing until Dec. 10, 2020. Register free
• Using up-to-date data ensures budget accuracy for clinical trials. • Budgets require tools for cost savings, defendable processes, and more. • GrantPlan enables budgeting teams to keep costs at fair market value.
• Managing the financial aspects of sponsor–payer–clinical site relationships • Case study and implications: investigator payments issues
This webinar will provide an overview of the Japanese regulations and development in the Japanese market. Live: Thursday, Oct. 31, 2019 at 11am EDT On demand available after airing until Oct. 31, 2020 Register free
Using AI/ML and advanced techniques in clinical development is more than just hype – it is greatly enhancing clinical trials today! Learn how pharmaceutical firms are realizing the benefits of better study design, faster recruitment, automated safety approaches and more informed, faster decision-making with risk-based and centralized monitoring. Live: Tuesday, Oct. 1, 2019 at 11am EDT On demand available after airing until Oct. 1, 2020. Register free: Register free
