Webcasts

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.

Thursday, September 30, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Give yourself a competitive edge by learning how the world’s leading designer of innovative clinical trials can help you integrate elements of economic theory to your clinical trial design. Optimize sample size, speed, and power by exploring a broader array of designs and quickly identifying those that meet your objectives.

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

Europe & US: Wednesday, September 22, 2021 at 1:30pm BST | 8:30am EDT Asia & US: Tuesday, September 28, 2021 at 7:30am CST | 4:30pm PDT This panel discussion will include a lively conversation with Parexel regulatory experts from USA, Europe, and China, who will address how to utilize simultaneous expedited approvals to accelerate global drug development.

Thursday, September 16, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST In today’s highly competitive clinical research landscape, Sponsors must be equipped to ramp up resourcing needs at a moment’s notice. This webinar will discuss proven recruiting techniques that pharmaceutical and biotechnology companies can apply today to attract more candidates and convince them to accept offers quickly – while creating an engaging employee experience for talent.

Wednesday, September 15, 2021 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST It’s with this in mind that we invite you to join us in an industry-first training and certification program that provides the specialized tools, knowledge, and skills necessary to develop and scale decentralized trials. Together, we can help codify new roles and learning paths that empower the industry to design, build, deploy and support decentralized trials. We can scale best practices and shared expertise to help trial teams break down traditional barriers, reduce cycle times, enhance data quality, and improve patient access and experience. But most importantly, in doing this we help scale a more inclusive scientific future for all.

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.

Tuesday, July 13, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

*** Thursday, June 17, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Join this webinar to hear best practices on how to enhance site-sponsor collaboration, compound efficiencies and accelerate trials by enabling end-to-end document exchange between sponsor eTMF systems and Florence’s leading eISF solution through Cognizant SIP. ***On demand available after final airing until June 17, 2022***

*** 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 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** It has never been more important for sponsors, monitors, and sites to learn how best to conduct monitoring visits remotely and securely. Learn about implementing remote monitoring, including analyzing implementation challenges, understanding the FDA’s guidance on delayed monitoring, and more. ***On demand available after final airing until May 26, 2022***

*** Monday, May 24, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Most organizations deal with the vulnerabilities that exclusive point solutions create. Join industry leaders Oracle and IQVIA to understand how inclusivity and a flexible environment can help you employ new approaches faster, and the benefits of collaboration in today’s clinical trials ecosystem.*** On demand available after final airing until May 24, 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***

*** Thursday, May 13, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Navigating the world of clinical trials and looking for the next best sourcing solution? Join Myonex’s Andrew Gregoire and Tom Gregson as they discuss key benefits to clinical trial prescription solutions. *** On demand available after final airing until May 13, 2022 ***