IQVIA Digital Site Suite

31. 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. 

32. 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.

33. 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.

34. Say It With Technology: How Alnylam Fosters A Connected Relationship With Sites 3/12/2021

    Alnylam Pharmaceuticals is developing an entirely new class of medicines and delivered the world’s first and only approved RNAi therapeutics in 2018 and 2019. Learn how Alnylam earned its reputation among investigators as a sponsor of choice by standardizing studies on a collaborative portal more than 6 years ago and leveraging technology to deliver results.

35. Navigating Complexities In Global Payment Operations: Best Practices For Sponsors 12/7/2020

    Deploying a successful global program for paying clinical research sites is an achievable and worthwhile goal but requires an understanding of the differences in frameworks and motivations. Learn what is needed to pays site globally in a reliable, timely, and equitable manner.

36. Global Pharma Company Dramatically Improves Collaboration, Communication, And Compliance In Trials 10/9/2020

    A Top 5 global pharmaceutical company wanted to help sites do everyday tasks more efficiently, making it easier for site staff to adhere to the protocol and deliver high-quality data. After evaluations and pilots, the company deployed an Investigator Site Portal in a 4-phase approach that delivered benefits each step of the way.

37. Best Practices For Site Communications During COVID-19 6/8/2020

    With so much new and updated information being shared on nearly a daily basis, it’s important to consider the most effective methods of organization and distribution. Here are some best practices we’ve compiled from working with sponsors and sites of all sizes and specialties during the COVID-19 pandemic.  

38. IQVIA Learning Management System 5/20/2020

    IQVIA’s Learning Management System (LMS) provides sites and study teams with a single, efficient source for education and learning, knowledge assessments, reporting and more.

39. IQVIA Safety Notifications 5/20/2020

    Now featuring cross-trial functionality, IQVIA Safety Notifications gives sponsors and contract research organizations (CROs) a centralized, simple solution for disseminating, managing, and tracking SUSARs and other safety notifications.

40. IQVIA Investigator Site Portal 5/20/2020

    IQVIA Technologies’ Investigator Site Portal (formerly DrugDev) offers sponsors, CROs, and sites the ability to manage trials easily and efficiently, from beginning to end, by enabling users to communicate effortlessly with sites, design and execute goals, and provide reporting, trial metrics, and much more.