Digital Site Suite OG
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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.
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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.
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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.
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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.
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Preventing Information Overload - Using Study Portals To Engage Site Staff
3/2/2020
For many sites, the overabundance of communications through email, system notifications, or other means isn’t just common, it’s standard. To combat this, sponsors have been using study portals to employ a traditional mix of best practices and tailored communication styles. This approach works because it covers the core needs of all clinical trial sites while also addressing the two different types of site users.
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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.
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Staying Connected In Crisis: Strong Site Communication Channels Stand Up To Pressure
4/14/2020
The COVID-19 pandemic is presenting unprecedented challenges to the clinical trial industry. Sites are in an unprecedented state of flux, and the pressure to understand the situation, protect patients and providers, and determine how to ensure continuity is on. Now more than ever, strong communication channels between sponsors and sites are critical.
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The Case For Patient Diversity In Clinical Trials
2/25/2021
Uncover how a global pharmaceutical company met the FDA's challenge to increase patient diversity with a multi-tiered approach combining key tactics and technology.
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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.
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The ROI Of IQVIA Site Payments
5/21/2020
This short video explains how and why business process outsourcing (BPO) using IQVIA Technologies for site payments offers excellent ROI for sponsors and peace of mind for sites and investigators.