Recent Webinars

31. 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.

32. 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.

33. 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.

34. 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.

35. 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.

36. Balancing Data, Technology, And Strategy In Clinical Research 6/11/2024

    Here, viewers will learn about best practices for developing an effective data collection strategy and selecting technology solutions that align with research needs.

37. Build Your Diversity Action Plan With AI And Patient Insights 5/29/2024

    Discover how AI and patient insights can help you build a compliant Diversity Action Plan and overcome barriers to achieve diverse clinical trial enrollment.

38. Technology Overload: Addressing Site Challenges Of Digital Trials 5/23/2024

    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.

39. Leveraging Multiple Data Sources For Comprehensive Insights 5/22/2024

    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.

40. The Synergistic Role Of Drug Safety In Clinical Trial Operations 4/25/2024

    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.