Newsletter | May 12, 2022

05.12.22 -- Deliver Relief To Struggling Sites

 

Global Pharma Company Dramatically Improves Collaboration, Communication, And Compliance In Trials

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. Read about a four-phase tech implementation that delivered benefits to sites each step of the way and gave the sponsor complete oversight.

Solutions
IQVIA Investigator Site Portal

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 all users to communicate and share documents effortlessly, design and execute goals, see trial metrics, and much more.

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Orchestrated Study Start-Up

Learn how the IQVIA Investigator Site Portal reduces activation timelines and eliminates site frustrations by automating processes and providing complete oversight to study teams.

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IQVIA Learning Management System

IQVIA’s Learning Management System (LMS) provides sites and study teams with a single, efficient source for cross-trial training and credits, with knowledge assessments, reporting, and more.

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IQVIA Safety Notifications

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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