Webcasts

November 3rd 2022 9 am CT |10 am ET | 2 pm GMT | 3pm CET The way clinical trials are conducted in the European Union is undergoing major changes with (EU) No 536/2014. 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.

Wednesday, October 26, 2022 at 2pm EDT|11am PDT|7pm BST|8pm CEST In this webinar, we will we review case studies of successful thought leader engagement plans across the product launch continuum to address the complexity including establishing a modeling framework early, incorporating thought leader behavior profiles and peer recognition data in addition to key milestone for creating the most efficient plan possible.

October 18th 2022 9 am CT |10 am ET | 3 pm BST | 4 pm CET Oracle’s market-leading safety software solutions provide highly powerful technology and algorithms for data mining. Combining Cerner Enviza’s real-world datasets containing de-identified, person-centric, longitudinal records offers a vast resource for expanding the potential of safety signaling.

Thursday, October 6, 2022 12 PM BST |1 PM CEST (Europe) Thursday, October 6, 2022 11 AM EDT | 8 AM PDT (US/CAN) Join IQVIA’s webinar exploring our first ever Global Incentive Compensation Benchmark Study including comprehensive feedback from a diverse group of IC professionals in the life sciences industry. Gain valuable information to maximize IC planning and execution that will equip field forces for current and future go-to-market success.

Wednesday, October 5, 2022, 11:00 AM ET Increase the value of your speaker programs with data and intelligence. Join IQVIA experts as they share industry trends and explain how modernizing this top performing channel by incorporating data, intelligence and the latest technology can help you adapt your engagement strategies for maximum impact.

October 4th 2022 9 am CT |10 am ET | 3 pm BST | 4 pm CET Managing drug, vaccine, and device safety has become increasingly challenging as companies are confronted with adverse event (AE) caseloads rising as much as 30-50% per year. Constrained resources and limited qualified outsourcing options have created the need to streamline the pharmacovigilance/multivigilance process.

Thursday, September 29,2022 at 11am BST | 12pm CEST | 6am EDT Learn how to utilize Advance Analytics and Machine Learning on integrated Real-World Data (RWD) to enhance your current understanding of the market to rapidly identify patients who can benefit from treatment. Hear experts explore several use cases including an interactive demo: from early opportunity patient finding and patient activation to brand positioning and contextualized HCP messaging of disease characterization.

Wednesday, September 28, 2022, 11 am ET Join this webinar to hear industry thought leaders discuss issues that impede cell and gene therapy development. They will cover new approaches for expanding viral vector manufacturing capacity with appropriate quality, share recommendations for streamlining clinical trial design and process development, explore opportunities for adapting the regulatory framework for cell and gene therapy technologies, and examine innovative pricing and contracting models.

Thursday, September 22, 2022 at 11am EDT | 8am PDT | 4pm BST |5pm CEST

Tue, Sep 20, 2022 10:00 AM EDT The seamless integration of data collected on patient behaviors and experiences is critical to improving the efficiency and effectiveness of clinical decision-making at scale in clinical research and development. Yet, the potential of sensor data to transform health outcomes is being held back by a fragmented landscape of device solutions, regulatory complexity, and obstacles in interoperability.

Wednesday, September 14, 2022 at 9 am EDT | 2 pm BST Join this webinar to learn more about how you can leverage the distinct value of the MDV database for your research in an increasingly global world. Easily gain a comprehensive view of a patient’s hospital health care history from one of the largest real-world databases in Japan. Explore de-identified claims, procedures, medications, and lab data, to help understand treatment patterns, clinical development, market access, and evidence generation.

Tue, Aug 30, 2022 11:00 AM EDT Demand for real-world evidence (RWE) is rising. But which data sources can meet the need for actionable RWE? EHR vs. registry data—which is better?

Wed, Aug 24, 2022 7:00 AM EDT he DARWIN EU Coordination Centre will accelerate access to high-quality real-world evidence for the use, safety and effectiveness of drugs across the EU in support of the EMA’s regulatory decision-making. By establishing a pan-European network, the DARWIN EU® will set standards for federated data analysis using a common data model to support the deeper integration of secondary data into regulatory decision-making as a complement to prospective clinical trials.

Tue, Aug 23, 2022 1:00 PM EDT Hear how Werewolf Therapeutics successfully transformed its spend management processes by driving efficiencies; increasing savings; and implementing efficient, compliant systems on a scalable foundation for growth. How do procurement and finance leaders at biopharma companies plan for a future that has unknowns and uncertainty? Hear Werewolf Therapeutics share insights, lessons learned, and key decision points that allowed the company to build mission-aligned, transformative value

Thu, Aug 18, 2022 2:00 PM EDT Value for patients, value for all. Learn how today’s health equity initiatives are shaping best-in-class clinical development frameworks of the future.

Wed, Aug 17, 2022 2:00 PM EDT Recent advances in both oncology drug development and novel digital technologies provide a ripe opportunity to enhance the clinical trial process. Join Colin Weller and Musaddiq Khan from Medable as they discuss the key considerations around these innovations.

Mon, Aug 8, 2022 1:00pm EST | 10:00am PST | 7:00pm CEST Real-world data networks are changing how data is collected and leveraged for evidence generation. A tech-enabled platform approach can significantly automate and reduce the burden of clinical study programs and registries, improve site and patient engagement and lower costs.

Thu, Jul 28, 2022 11:00 AM EDT With no cure for IBD and other conditions, like NASH, treatments are aimed at reducing symptoms and preventing complications. Real-world data and AI applications provide a unique opportunity to better understand disease progression, treatment effectiveness, and outcomes.

Thursday, July 21st 2022 at 11am EST, 8am PST, 5pm CEST Join this webinar to hear industry thought leaders discuss how data and experiences serve clinical and commercial needs, explore which platforms and technologies can enable a robust digital health ecosystem, and share recommendations for building a digital health strategy fit for your business.

Now Available On Demand! What is key learning? Over 50% of industry forecasters said they would like better access to one key thing. Join us to discuss this important finding and more from our IQVIA Commercial Forecasting Trends Survey.

Now Available On Demand! HCP engagements remain the single-most valuable way to provide information needed by HCPs to effectively prescribe the best treatments for their patients. However, the complexities of managing these engagements are burdensome and complex. In this webinar, learn the keys to navigating this increasingly complex space while enabling optimized, worry-free engagements with exceptional HCP experiences.

Now Available On Demand! Join this webinar to learn a new way to quickly identify the right real world data sources. IQVIA Health Data Catalog makes assessing RWD fast and easy with 2000+ unique global data assets, 200+ variables describing patient data, and up-to-date profiles to efficiently compare which is most relevant for your project.

Wednesday June 15, 2022 from 11am EDT | 8am PDT| 4pm BST | 5pm CEST IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections to deliver powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 74,000 employees, IQVIA conducts operations in more than 100 countries. Learn more at www.iqvia.com.

Now available on demand! Medical affairs is a high visibility role with a heavy lift to both to engage the right HCPs and KOLs as well as bring strategic, data-driven value to their organizations. But what no one saw coming was a pandemic that would change everything: the ways MSLs prepared; engaged; and strategized as well as an enhanced focus on driving HCP behavior that will have real-life downstream impact on patient outcomes. It’s a tall order. Join us to discuss what happened, where it’s going and how measurable impact has shifted.

Thursday June 8, 2022 at 11am PDT | 2pm EDT | 7pm BST | 8pm CEST Learn how life sciences companies can navigate growth by leveraging NetSuite for streamlined processes, better management reporting, and stronger financial controls to ensure real-time management decision-making and regulatory compliance.

Now Available On Demand! Building the best! Learn how to leverage real-world evidence and the newest patient insights to ensure you are building the most comprehensive, compliant, and diverse clinical trials.

Wednesday, May 18, 2022 at 5pm EDT | 10 pm (CET) Join IQVIA to gain insights into the key milestones on the roadmap to commercial success in Japan

Thursday, May 12, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Learn about the key facets of a strong and effective enterprise data management strategy for large, multinational pharma companies along with insight into how IQVIA is uniquely positioned to help with data, technology, and services.

Wednesday, May 11, 2022 at 2pm EDT | 11am PT | 7pm BST | 8pm CEST As physician customers become more difficult to access via traditional personal selling, brands are rethinking how omnichannel marketing can be leveraged to create a seamless customer experience while keeping the representative at the center of communication.

Thursday, April 28, 2022 at 11am PDT | 2pm EDT Are you ready for the challenges of going public? Whether you are a fast-growing biotech company or are currently public and looking for SOX compliance, this webinar will cover how to set up scalable and compliant financial processes.