IQVIA Digital Site Suite

31. Sky-High Inflation And The Great Resignation: The Impact On Clinical Site Budgeting 11/17/2022

    When it comes to negotiating budgets for a clinical trial, sponsors, CROs and sites all have the same goal: to run the study. Yet just like most business relationships, the conflict comes in what defines a fair price for services rendered. Now, with inflation at its highest rate in four decades and attrition rates at clinical research sites exceeding most industries, developing fair marketing value (FMV) for investigator grants is more contentious than ever.

32. The IQVIA Investigator Site Portal 11/15/2022

    Understand why companies are standardizing operations on a purpose-built, proven platform that empowers sites to succeed and provides sponsors with helpful insights.

33. IQVIA Feasibility 9/27/2022

    Employing a digital, data-first strategy, IQVIA Feasibility brings together survey data, confidential disclosure agreements (CDAs) and site intelligence data, enabling sponsors to efficiently collect vital information while improving the site experience.

34. Advanced Tech Can Thwart Site Staffing Problems 7/6/2022

    In clinical research, staffing shortages can delay trials and prevent new therapies from getting to patients in need. Read why Melissa Easy, VP, Clinical Technologies at IQVIA, believes advanced tech may bridge this gap as she reviews tools that are proving useful to study teams.

35. 3 Key Functions Your eTMF Needs To Meet New EMA Regulations 6/23/2022

    The European Union Clinical Trial Regulation No. 536/2014 recently introduced the most significant changes to the processes for clinical trial applications in at least the past 15 years. Learn how this impacts the Trial Master File and consider three key functions that an electronic TMF must have to achieve compliance and maintain organizational success.

36. How An AI/ML Data Strategy Can Deliver Better Business Outcomes 2/22/2022

    Discover how data science and artificial intelligence and machine learning driven predictive and prescriptive insights can help research teams cut the time and cost.

37. Elevating The Site-Sponsor Experience: SaaS-Based Feasibility And Site Selection For Clinical Trials 2/1/2022

    In this webinar, learn about the transformation clinical trial feasibility and site selection across the industry.

38. The Electronic Trial Master File: Study Item And Placeholder Analysis 5/21/2021

    Electronic trial master file (eTMF) systems are proving to be effective in planning, managing, monitoring, and maintaining inspection-readiness and compliance. Explore the use of planning wizards and how placeholder creation promotes study completeness, timely document uploading, and reduced rates of quality control failures. 

39. Simplifying And Empowering Oversight With IQVIA eTMF 5/21/2021

    The IQVIA eTMF is easy to use, quick to implement, and adaptable to the needs of growing biotechs. Take control of compliance and deliver seamless inspections with the IQVIA eTMF.

40. IQVIA eArchive 5/21/2021

    Whether you’re archiving a TMF delivered by your CRO partner, looking to move out of noncompliant file systems, or interested in reducing the high costs of archiving in your active eTMF, IQVIA eArchive is the rapid deployment solution for you.