IQVIA

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.

Thursday April 28, 2022 at 11 am ET In this webinar, IQVIA experts will share how to harness data, technology, and advanced analytics to inclusively recruit the right patients in the right places at the right time into Alzheimer’s disease clinical trials.

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.

Nagaraja Srivatsan, SVP & Chief Digital Officer at IQVIA, breaks down the most recent challenges in the decentralized trial space: patient burden, the ecosystem between the patient and information, and the global regulatory landscape.

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.

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.

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.

February 17, 2022 11am EST Learn how the most forward-thinking sponsors are using data and analytics to personalize study experiences, including identifying patients of interest, and streamlining outreach strategies to eliminate barriers to participation. Join IQVIA experts for an insightful webinar on “Patient-centric trials done right - Transforming a generic one-size-fits-all experience into an agile environment adapted with data and technology,” where you’ll hear how to leverage technology to identify the intended patients, refine engagement, and optimize trial outcomes.

Wednesday, February 16, 2022 at 11am EST Are duplicative and voluminous safety letters from your clinical trials overwhelming investigators and staff? See how the Safety Notifications module of the IQVIA Investigator Site Portal can ease the administrative burden and put the focus back on patient safety in this complimentary webinar from IQVIA Technologies.

Tuesday, February 1, 2022 at 11:00 EST What is key learning? Can adaptive trials ensure quicker decision-making? Can the added value of running adaptive trials be measured?

Wednesday, January 26, 2022 at 11am EST Are your feasibility assessments repetitious and frustrating for everyone involved? See why sites are already saying they are “highly satisfied” with an all-new Feasibility module from IQVIA Technologies in this complimentary webinar.

Tuesday, November 30th, 2021 at 11am EST Current changes in technology and the impact of the COVID pandemic has greatly accelerated the adoption of RBM methodology and AI/ML assisted risk analysis. How are these changing directly impacting your future clinical trials as the industry is reorienting itself around a new normal with regards to monitoring and insights provided by integrated data reviews.

Tuesday, November 9, 2021 11 am EST | 8am PST | 5pm CET | 4pm GMT Learn how to strengthen patient engagement, improve data quality, and drive greater efficiency in your next clinical trial using decentralized clinical trials tools and eCOA.

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.