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IQVIA

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18 reviews
  • 6 profiles
  • 8 categories
Average star rating
4.3
Serving customers since
2016

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IQVIA eTMF

0 reviews

IQVIA eTMF is an advanced electronic Trial Master File solution designed to streamline the management of clinical trial documents. By integrating precision planning with intelligent automation, it ensures that trial master files are consistently inspection-ready, thereby enhancing compliance and operational efficiency. The platform's intuitive design minimizes manual efforts, reduces risks, and provides real-time insights into document quality, timeliness, and completeness. This empowers clinical teams to proactively address issues, maintain continuous audit readiness, and keep studies on track. Key Features and Functionality: - Intelligent Automation: Automates document classification, quality control checks, and finalizations, reducing manual workload and potential errors. - Real-Time Dashboards: Provides immediate insights into eTMF health through customizable dashboards, enabling proactive management of document quality, completeness, and timeliness. - Study Set-Up Wizards: Facilitates rapid initiation of new eTMF study environments with minimal clicks, guided by intuitive wizards. - Site Zone: Simplifies document exchange between sites and sponsors without requiring additional integrations, enhancing collaboration. - eTMF Expert Services: Offers specialized support to manage, monitor, and maintain eTMF workflows, ensuring alignment with quality assurance standards. - eTMF Archive: Ensures long-term compliance by securely archiving completed trials, with cost-effective solutions independent of site volumes. Primary Value and User Solutions: IQVIA eTMF addresses the complexities of managing trial master files by providing a centralized, automated platform that enhances compliance and operational efficiency. It reduces manual tasks, mitigates risks, and ensures continuous inspection readiness. By offering real-time insights and streamlined workflows, it empowers clinical teams to maintain control over document management, improve collaboration between stakeholders, and ultimately accelerate the clinical trial process.

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IQVIA

14 reviews

IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

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SmartSolve

4 reviews

SmartSolve, Pilgrims powerful suite of quality management software solutions, is engineered for the Life Sciences. Delivered on a compliance-ready platform, SmartSolve provides closed-loop process integration unmatched in the market

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AHM CentrisDirect

0 reviews

AHM Centris Direct is an end-to-end platform suite to manage compliant interactions with healthcare professionals and organizations.

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IQVIA eTMF

0 reviews

IQVIA eTMF is an advanced electronic Trial Master File solution designed to streamline the management of clinical trial documents. By integrating precision planning with intelligent automation, it ensures that trial master files are consistently inspection-ready, thereby enhancing compliance and operational efficiency. The platform's intuitive design minimizes manual efforts, reduces risks, and provides real-time insights into document quality, timeliness, and completeness. This empowers clinical teams to proactively address issues, maintain continuous audit readiness, and keep studies on track. Key Features and Functionality: - Intelligent Automation: Automates document classification, quality control checks, and finalizations, reducing manual workload and potential errors. - Real-Time Dashboards: Provides immediate insights into eTMF health through customizable dashboards, enabling proactive management of document quality, completeness, and timeliness. - Study Set-Up Wizards: Facilitates rapid initiation of new eTMF study environments with minimal clicks, guided by intuitive wizards. - Site Zone: Simplifies document exchange between sites and sponsors without requiring additional integrations, enhancing collaboration. - eTMF Expert Services: Offers specialized support to manage, monitor, and maintain eTMF workflows, ensuring alignment with quality assurance standards. - eTMF Archive: Ensures long-term compliance by securely archiving completed trials, with cost-effective solutions independent of site volumes. Primary Value and User Solutions: IQVIA eTMF addresses the complexities of managing trial master files by providing a centralized, automated platform that enhances compliance and operational efficiency. It reduces manual tasks, mitigates risks, and ensures continuous inspection readiness. By offering real-time insights and streamlined workflows, it empowers clinical teams to maintain control over document management, improve collaboration between stakeholders, and ultimately accelerate the clinical trial process.

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IQVIA RIM Smart

0 reviews

IQVIA RIM Smart is a comprehensive Regulatory Information Management (RIM solution designed to streamline and enhance regulatory processes for life sciences organizations. It offers a unified platform that integrates various regulatory functions, enabling efficient management of product registrations, submissions, and compliance activities. Key Features and Functionality: - Centralized Regulatory Data Management: Provides a single source of truth for all regulatory information, ensuring data consistency and accuracy across the organization. - Submission Planning and Tracking: Facilitates the planning, preparation, and tracking of regulatory submissions, improving efficiency and reducing time to market. - Compliance Monitoring: Automates compliance checks and monitors regulatory requirements to ensure adherence to global standards. - Workflow Automation: Streamlines regulatory workflows through automation, reducing manual efforts and minimizing errors. - Reporting and Analytics: Offers robust reporting tools and analytics to provide insights into regulatory activities and support informed decision-making. Primary Value and User Benefits: IQVIA RIM Smart addresses the complexities of regulatory management by providing a centralized and automated solution that enhances efficiency, ensures compliance, and accelerates time to market for life sciences products. By integrating various regulatory functions into a single platform, it reduces manual efforts, minimizes errors, and provides real-time visibility into regulatory activities, enabling organizations to make informed decisions and maintain a competitive edge in the industry.

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IQVIA

0 reviews

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences and healthcare industries. Formed through the merger of IMS Health and Quintiles, IQVIA leverages its extensive data resources, cutting-edge technologies, and deep domain expertise to drive healthcare innovation and improve patient outcomes. Key Features and Functionality: - Research & Development Solutions: IQVIA offers comprehensive clinical trial management services, including project management, clinical monitoring, patient recruitment, and data management, facilitating efficient and effective clinical development processes. - Real World Evidence: The company provides real-world data and evidence generation services, enabling clients to make informed decisions by analyzing patient outcomes and treatment patterns. - Commercialization Services: IQVIA delivers strategic consulting, market analytics, and sales force effectiveness solutions to optimize product launches and commercial performance. - Technology Solutions: With a suite of cloud-based applications and AI-driven analytics, IQVIA supports data integration, customer engagement, and performance management across the healthcare ecosystem. - Compliance and Regulatory Services: The company offers integrated compliance solutions, including regulatory affairs, pharmacovigilance, and quality management, ensuring adherence to global healthcare regulations. Primary Value and User Solutions: IQVIA's integrated solutions empower pharmaceutical, biotechnology, and medical device companies to accelerate drug development, enhance commercial success, and maintain regulatory compliance. By harnessing vast datasets and advanced analytics, IQVIA helps clients uncover insights that drive innovation, improve patient care, and achieve better health outcomes worldwide.

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IQVIA Reviews

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Profile Name
Star Rating
10
8
0
0
0
AS
Ajit S.
10/12/2025
Validated Reviewer
Verified Current User
Review source: G2 invite
Incentivized Review

Best enterprise quality management software

integration with other platforms, customization as per requirement, Easy reporting, customized dashboard, role management, single sign-on
Verified User in Medical Devices
UM
Verified User in Medical Devices
07/09/2024
Validated Reviewer
Verified Current User
Review source: G2 invite
Incentivized Review

Overall a robust sofware system

Being able to organize and store all our training and SOP/work instructions in one place. Updating them with changes is much easier with SmartSolve
NG
NITIN G.
03/14/2024
Validated Reviewer
Review source: G2 invite
Incentivized Review

Best eQMS solution

Help in proper maintanence and tracking of complaints, CAPA, NC, devitations, inspection reports etc. Its very easy to use and we use it on a daily basis. It can be integrated easily with other tools

About

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HQ Location:
Durham, US

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@IQVIA_global

What is IQVIA?

IQVIA is a global leader in the field of advanced analytics, technology solutions, and contract research services for the life sciences industry. By leveraging its extensive expertise and integrated data solutions, IQVIA aids in the transformation of healthcare by enabling clients to harness data-driven insights to optimize their clinical development and commercialization processes. The company offers a broad range of services including real-world insights, clinical trial management, and regulatory consulting, helping pharmaceutical, biotech, and medical device companies innovate and improve patient outcomes.

Details

Year Founded
2016
Ownership
NYSE: IQV