Webcasts

Now Available On Demand! Learn best practices to optimize your clinical supply chain management to decrease costs, improve productivity, and increase patient retention for a more successful clinical trial.

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

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.

Thursday, May 12, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Many organizations have yet to figure out how to fit digital, hybrid, and decentralized clinical trial methods into their existing ecosystems in a scalable and efficient way. This webinar will go through the complexities that decentralized and hybrid methodologies bring to first-generation platforms, and how a single, unified platform enables interoperability and flexibility to help truly unlock the potential of these digital study methods.

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.

Tuesday, May 3, 2022 at 11am EDT | 7am PDT | 3pm BST | 4pm CEST What can the eClinical technology industry learn from consumer-focused technology companies? They can learn effective approaches that help engage, incentivize, and motivate patients in clinical trials, to improve recruitment and decrease attrition.

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.

Tuesday, April 12, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST ** Tuesday, April 19, 2022 at 8:30am CST | 5:30pm PDT | 8:30PM EDT This webinar will include an educational session with Parexel experts, who will address how to build an evidence strategy for your cancer drug that is both approvable and reimbursable.

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.

Thursday, March 17, 2022 at 2pm EDT | 11am PT | 6pm GMT | 7pm CET Oncology trials of the future are enriched with real-world data. Learn how to unlock better patient outcomes, faster research, and lower healthcare costs by combining a SaaS DCT platform with real-world data connectivity.

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.

Wednesday December 8, 2021 at 11am EST | 8am PST | 4pm GMT | 5pm CET Join this webinar to learn how to approach the early stages of drug development and build a long-term plan to advance your drug to market.

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.

Now Available On Demand! In this webinar, we will explore best practices to optimize your protocol, country and site feasibility strategy by employing a robust multi-channel strategy and a risk management feedback loop to monitor and mitigate risks throughout the project.

Available On Demand This panel discussion will include an informative conversation among Parexel experts, who will share key considerations in accelerating drug development for rare diseases.

Now Available On Demand! The Next Generation Central Lab is on its way. Frontage Laboratories Inc explains how it envisions the next-generation central lab and what it will take to get there.

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.

The way clinical trials are conducted in the European Union will undergo a major change when (EU) No 536/2014 comes into effect in January 2022. But just being compliant with the regulation should not be considered enough – forward-looking organizations are rethinking how technology can play an important part in bringing efficiencies to clinical trials, by reducing failures and driving operational changes beyond compliance.

***Live: Tuesday, October 26, 2021 at 11 EDT | 8am PDT | 5pm CEST | 4pm BST*** Oracle Health Sciences reveals new research conducted to understand the technology adaptations that were made to clinical trials during the pandemic, the effect of these adaptations, and the impact of these changes on the future of clinical trials.

Monday, October 25, 2021 at 10am EDT Attend this webinar to hear about CGP, the latest in onco-innovation for genomic biomarker testing and uncover the role that Illumina and Q2 Solutions are playing in evolving the CGP testing landscape to deliver a localized testing model to support oncology precision medicine clinical trials in Europe. Lastly, the webinar will reveal the updated roadmap of Q2 Solutions’ Edinburgh Genomics laboratory.

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.