Optimized Clinical Trials: A “From the Field” Webinar
November 16th 2022Part 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.
Using IRT Data to Automate and Optimize Clinical Supply
November 9th 2022Wednesday, 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
Turn Real-World Data Insights Into a Personalized Trial Journey for Every Patient
November 2nd 2022Part 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.
eConsent for complex clinical trials
September 20th 2022Tuesday, 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.
Transforming Data Into Insights and Outcomes in Risk Based Quality Management (RBQM)
September 13th 2022Tue, 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.
Maximize Your Early Phase Oncology Assets with a Successful Drug Development Plan
July 27th 2022Wed, 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.
Ensuring Data Quality in a Complex Trial Landscape
July 26th 2022Tue, 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.
Redefining Patient Centricity: Next Best in People, Processes and Technology in DCTs
June 9th 2022Watch 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.
Integrated Monitoring: Applying technology and analytics to drive monitoring efficiencies
May 26th 2022Thursday, 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
Effective Scenario Planning for Drug Development: A Conversation With Experts
May 5th 2022Now 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.
Moving Science Forward in Alzheimer’s Disease Clinical Trials
April 28th 2022Thursday 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.
The Top 3 Technological Challenges in Decentralized Trials
April 20th 2022Nagaraja 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.
BYOD is Here to Stay: Considerations for implementing a BYOD eCOA strategy
March 22nd 2022Tuesday, 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.
Elevating the Site-Sponsor Experience: Learning Management SaaS in Clinical Trials
March 9th 2022Wednesday, 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.
Clinical Data Flow: The Foundation of a Biostatistics Ecosystem within a Data Universe
February 24th 2022Thursday, 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.