RECENT WEBINARS
Rethinking Effectiveness In Clinical Operations: Balancing Tradeoffs In An Era Of Disruption
In an era defined by rapid disruption and technological advancement, clinical operations leaders are under increasing pressure to enhance effectiveness while managing complex strategic trade-offs.
How To Select The Right Bioanalysis CRO For Your Program
The right bioanalysis CRO acts as a strategic accelerator, while the wrong one can slow progress and jeopardize outcomes. But when every provider promises speed and credibility, how can you confidently identify the right partner?
Unlock Peak Performance: AI-Powered Study Start-Up And Execution
In part two of our webinar series, speakers delve into how artificial intelligence is reshaping every stage of the clinical trial journey — from designing smarter, more feasible protocols to streamlining study start-up and execution.
From First-In-Human To Proof-Of-Concept — Quicker, Smarter, Streamlined
Explore examples of smarter SAD/MAD trial designs including multi-part and hybrid protocols, regulatory foresight, recruitment considerations, and operational strategies that keep programs moving.
How ICH Oversight And AI Are Shaping The Future Of Clinical Trials
Explore how the new ICH E6 (R3) revisions are reshaping clinical trial oversight and examine how AI-driven tools like the Clinical Decision Suite can help sponsors enhance trial efficiency.
The End Of Clinical Trial-And-Error: AI-Powered Design For Protocol Certainty
Discover how AI-powered predictive analytics and protocol optimization tools can improve trial feasibility, forecast patient enrollment, and reduce burden.
Avoid The Wrecking Ball: Targeted Solutions For Struggling Trials
In this presentation, our expert panel introduces the concept of scaffolding — a targeted reinforcement strategy designed to strengthen trials from the inside out.
Ensuring Compliance In Gene Therapy Trials: IRB And IBC Views
Explore ethical and regulatory challenges in neurological gene therapy trials, with expert insights on IRB/IBC collaboration, consent protocols, and oversight for vulnerable populations.
Bridging The Gap: EHR To EDC Integration In Clinical Trials
This distinguished panel of industry experts shares an engaging and honest discussion about the current state and future potential of EHR-to-EDC integration.
Breaking Barriers With PCR: Innovative Solutions For Clinical Trial Success
This presentation brings together experts from Precision for Medicine, Avidity Biosciences, and Indaptus Therapeutics to examine the expanding role of PCR-based molecular monitoring.
The Strategic Advantage of Australia And Asia for U.S. Biotechs
This expert panel explores how Australia, Taiwan, and South Korea provide a strategic advantage in conducting early, mid, and late-phase oncology trials.
Fixing The Monitoring Model: Flexible Resources For Trial Success
Discover how flexible, site-focused monitoring strategies are transforming clinical trials by improving communication, enhancing compliance, and resolving challenges before they impact study success.
The Role Of Technology In Improving Site Performance
Explore how clinical trial sponsors can benefit from the growing use of electronic source (eSource) technology at research sites.
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.
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.