RECENT WEBINARS
Embedding AI And Critical IRB Operations Data To Drive Intelligent Study Design
Explore how modern clinical trial design is being transformed by a rich array of data sources through this clear roadmap for navigating the evolving complexities of the industry.
CRO Selection Science: Insights From $2B+ Vendor Choices
Discover how data-driven strategies and structured RFPs can simplify CRO selection, improve transparency, and ensure the right operational fit. Learn practical steps to make smarter vendor decisions.
Should Sponsors Provide Source Document Templates?
Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.
EU GMP Annex 11: Compliance Strategy And Digital Solutions
Explore how EU GMP Annex 11 revisions could reshape global pharmaceutical compliance, as well as strategies for navigating implementation challenges and building future-ready validation programs.
Rethinking Effectiveness: 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 accelerates progress, while the wrong one can derail outcomes. When every provider claims speed and credibility, how do you confidently choose 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.
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.