IQVIA

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.

Tue, Nov 15, 2022 11:00 AM EST Learn how people, process and technology all contribute to successful implementation of RBQM technology.

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

Tue, Nov 8, 2022 11:00 AM EST Join the webinar to explore next generation technologies, and devices to evaluate respiratory functions in Decentralized Clinical trials, keeping patient centricity at the core.

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.

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

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, 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.

Watch our roundtable participants discuss the Next Best in Patient Centricity, with topics including the meaning of patient centricity; how to increase patient engagement in clinical trials; data and technology; and the site perspective.

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.

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

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.