Name: IQVIA Trial Management Suite
Author: IQVIA

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The IQVIA Trial Management Suite is a solution designed to optimize efficiency and enhance trial outcomes in the field of clinical trials. According to IQVIA, this suite seamlessly integrates best-of-breed, modular, interoperable technologies to streamline trial management processes, facilitate real-time collaboration, and provide centralized access to study documentation. The suite caters to companies of various sizes, ranging from small and mid-sized organizations to large enterprises. Clinical research professionals, clinical trial managers, pharmaceutical companies, contract research organizations (CROs), and academic research institutions are among the many professions and industries that can benefit from this suite.

## Key Features

**Digital Trial Management Suite**: According to IQVIA, this suite allows for seamless orchestration of clinical trials with an innovative CTMS and dynamic monitoring, streamlining trial management processes from start to finish.

**Digital Site Suite**: IQVIA claims that this suite increases transparency and reduces administrative burden for all stakeholders by enabling seamless collaboration between sponsors and sites through a user-friendly web portal.

**Planning Suite**: IQVIA states that this suite accurately predicts study timelines, budgets, and performance, optimizing study design decisions and resource allocation through advanced analytics and predictive modeling.

**Patient Engagement Suite**: According to IQVIA, this suite simplifies the trial experience for participants and enhances engagement and retention through technology-driven solutions, including remote data collection, ePRO, and eConsent.

**Clinical Data Analytics Suite**: IQVIA claims that this suite harmonizes data and leverages AI technologies to generate actionable insights, improving trial efficiency, accelerating filings, and enhancing data quality and integrity.

**Integrated IRT eCOA Solution**: According to IQVIA, this suite improves study quality and reduces site and sponsor burden by integrating IRT and eCOA solutions, streamlining data flow and simplifying user creation.

The Trial Management Suite (TMS), part of IQVIA Technologies Orchestrated Clinical Trials (OCT) platform, is composed of several applications integrated from the start and powered by an industry leading, cloud-based platform. The SaaS-based applications are interoperable with existing systems and are designed to help accelerate traditional, hybrid and decentralized trials with a risk-based strategy.

The MasterControl Quality Excellence suite bundles a number of products supporting work quality and compliance including training and exams, incidents and corrective actions (CA), documents and change, and other modules.

MasterControl Quality Excellence

IQVIA Trial Management Suite

A Clinical Trial Management System(CTMS) supports research institutes and pharmaceutical to run clinical studies with human subjects. Therefore they store subject information and support research operations with planning, benchmarking, and reporting features, and also should integrate with a business intelligence or analytics platform, if it does not contain such features intrinsically.

Clinical Trial Management

IQVIA

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IQVIA Trial Management Suite

Overview

What is IQVIA Trial Management Suite?