RECENT WEBINARS
Mastering The Complexities Of Gene Therapy Document Writing
Gain the insight and strategic flexibility needed to confidently navigate the unique scientific, regulatory, and documentation challenges of gene therapy development.
Accelerating Clinical Data Review With Traceable Workflows
Discover how streamlined workflows and enhanced collaboration between data managers and medical reviewers can boost clinical trial efficiency, improve data quality, and ensure patient safety.
Critical Imaging Risks In GLP-1 And Neurology Studies
In the evolving landscape of GLP-1 and neurology clinical trials, imaging has become a pivotal tool for evaluating both efficacy and safety. Delve into the early indicators of imaging-related challenges and insights into preclinical strategies for effective risk mitigatio...
Inspection Readiness For Decentralized Trials
Decentralized Clinical Trials (DCTs) enhance research inclusivity by minimizing logistical barriers such as travel, scheduling conflicts, and costs, making participation more accessible.
Who's In Charge? How To Ensure Effective Trial Oversight, Leadership
Gain valuable insights into the role of sponsor-side Clinical Operations leadership, the risks of over-relying on CROs, and key strategies for fostering collaboration between sponsors and partners.
Introducing A Smarter, More Cost-Effective Way To Run Clinical Trials
While early-phase trials often rely on less capable, cost-effective systems, the transition to more complex studies in later phases necessitates a more robust EDC system.
Discovery Through Commercialization: A Biologic Drug's Analytical Journey
Gain valuable insights into advanced methods and analysis techniques for high-order structure, physiochemical characterization, cell-based and biochemical assays, and more.
Balancing Innovation, Ethics, and Operational Excellence in Adaptive Oncology Trials
Experts discuss how to navigate the complexities of adaptive trial designs and how ethics reviews uphold patient safety, ensure informed consent, and provide robust oversight.
Step Inside IQVIA One Home for Sites™
Whether you're a sponsor, site, or technology vendor, now is the time to embrace One Home and join this industry-wide collaboration.
Can We Enable Clinical Trials Operations Without Human-In-The-Loop?
In this presentation, panelists invite you to rethink traditional approaches, consider innovative risk mitigation strategies, and envision a future where clinical trials are not only faster and more efficient but also potentially free from human limitations.
Tailoring IRT/RTSM Solutions To Overcome Challenges
Learn how RTSM can be tailored to meet precision medicine’s unique challenges of expiry, visit & personalized shipment management.
Uncovering The Root Cause Of Clinical Trial Troubles
Discover essential strategies to prevent clinical trials from reaching a crisis while gaining a deeper understanding of the importance of addressing systemic issues early.
Digging Through The Hype: Can AI/ML Assist Clinical Development?
AI has great potential to enhance the efforts of your team members by accelerating data interactions. Watch this webinar and discover how AI can improve clinical trial outcomes and data management.
Unleash The Power Of IQVIA Complete Consent
Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.
5 Strategies To Dramatically Improve Clinical Data Quality
Discover how to unify data management and risk-based quality management approaches and augment processes with automation and AI to find and fix data quality issues sooner and more efficiently.
Reducing Risks By Outsourcing OSD Manufacturing And Packaging
Watch to discover the key benefits of outsourcing your OSD production and explore real-world examples and best practices to help you streamline your processes and enhance your operational agility.
Maximize Control And Transparency On The Path To Study Go-Live
Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.
From Crisis To Confidence: Ensuring Smooth Regulatory Submissions
Explore some of the major challenges that medical writing submission specialists face today and strategies that can consistently set the stage for success.
Impacting Sustainability Through Vendor Collaboration, Procurement
Guido D’Agostino, Head of Global Procurement at Chiesi, and Stefan Dürr, Senior Director of Product Management and Client Delivery at IQVIA IRT, delve into their achievements in sustainability.
Unleash The Power Of IQVIA eCOA: A Deep Dive
Edward Bartels, an expert in eCOA solutions, provides an in-depth overview of the market trends, emerging technologies, and how IQVIA eCOA is pioneering advancements in this space.
Revolutionizing Patient Recruitment For Clinical Research Sites
Understand key learnings from the site perspective on how to empower your principal investigators better and study coordinators to efficiently and effectively enroll patients for your trial.
Ensuring Effective PV Regulatory Intelligence With FSP Partnerships
Gain insights into what to look for in an FSP PV partner who can provide solid regulatory expertise and effective safety reporting across pharmaceutical, biotech, and medical device development.
Balancing Data, Technology, And Strategy In Clinical Research
Here, viewers will learn about best practices for developing an effective data collection strategy and selecting technology solutions that align with research needs.
Build Your Diversity Action Plan With AI And Patient Insights
Discover how AI and patient insights can help you build a compliant Diversity Action Plan and overcome barriers to achieve diverse clinical trial enrollment.
Technology Overload: Addressing Site Challenges Of Digital Trials
Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.
Leveraging Multiple Data Sources For Comprehensive Insights
Discover how integrating internal and external data can enhance decision-making and efficiency, how to manage diverse data sources, and the benefits of a single source of truth for your organization.
The Synergistic Role Of Drug Safety In Clinical Trial Operations
Delve into the significance of adept interpersonal leadership within your drug safety program, shedding light on the operational and financial benefits that stem from fostering a collaborative environment.
Case Study: Optimizing Clinical Supply Chain With Advanced Technology
In this interactive discussion, IQVIA Technologies' IRT experts delve into real-world examples and practical AI applications.
An Introduction To One Home for Sites™
This on-demand webinar provides a thorough overview of why IQVIA Technologies is building One Home for Sites, how it works, and who should participate.
Advancing Development Of New Oncology Therapies
Learn how the FDA's Project FrontRunner expedites cancer drug approval for early advanced metastatic cancer, emphasizing efficacy and safety in earlier clinical settings.