Recent Webinars

31. Digging Through The Hype: Can AI/ML Assist Clinical Development? 11/14/2024

    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.

32. Unleash The Power Of IQVIA Complete Consent 11/12/2024

    Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.

33. 5 Strategies To Dramatically Improve Clinical Data Quality 10/29/2024

    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.

34. Reducing Risks By Outsourcing OSD Manufacturing And Packaging 10/23/2024

    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.

35. Maximize Control And Transparency On The Path To Study Go-Live 10/10/2024

    Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.

36. From Crisis To Confidence: Ensuring Smooth Regulatory Submissions 10/8/2024

    Explore some of the major challenges that medical writing submission specialists face today and strategies that can consistently set the stage for success.

37. Impacting Sustainability Through Vendor Collaboration, Procurement 9/12/2024

    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.

38. Unleash The Power Of IQVIA eCOA: A Deep Dive 9/10/2024

    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.

39. Revolutionizing Patient Recruitment For Clinical Research Sites 8/28/2024

    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.

40. Ensuring Effective PV Regulatory Intelligence With FSP Partnerships 6/25/2024

    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.