IQVIA Vigilance PLATFORM

Improve quality, reduce costs, and access data for every phase of the safety lifecycle.

Over 3000 safety professionals in more than 100 countries.


The IQVIA Vigilance Platform is a drug safety system: a SaaS safety and pharmacovigilance platform that supports, streamlines, and enhances every phase of the safety lifecycle, driving down costs, improving quality and giving you easy access to your data. The result is greater efficiency, greater flexibility, greater insights and a platform built for pharmacovigilance automation and continuous improvement.

Your comprehensive, flexible, automated drug safety system

The flexible design of IQVIA Vigilance Platform lets you deploy the modules you require, adding features and functionality as your organization evolves. With AI at its core, the IQVIA Vigilance Platform enables near “touchless” processing while providing you seamless access to your data.

IQVIA Vigilance Intake

Automated processing of incoming adverse events with secure source handling, dictionary coding, full data review and follow-up identification/merge.

IQVIA Vigilance Case

Streamline operations and compliance with single-source-of-truth case processing, assessment and submissions for global and local teams.

IQVIA Vigilance Periodics

Deliver full lifecycles periodics reporting and workflow management to meet global regulatory obligations.

IQVIA Vigilance Analytics

Maintain oversight and real-time insights with drill-down queries, reporting libraries, operational dashboards and compliance metrics.

IQVIA Vigilance Detect

Auto-identify adverse events and product risks across diverse multi-lingual data sources (including social channels and audio formats).

IQVIA Vigilance Collect

Adverse events collection directly from reporters and patients (multi-lingual and mobile-enabled).

IQVIA Vigilance Signal

Automate real-time signal detection for proactive, adaptive safety surveillance and risk management across diverse datasets.

IQVIA Vigilance Administration

Deliver full life-cycle configuration capabilities to manage PLS and user security.
A transformational approach
The IQVIA Vigilance Platform reduces costs throughout the pharmacovigilance lifecycle. It is supported by expert consultants with decades of industry expertise. IQVIA’s 3000+ safety professionals in more than 100 countries interact daily with customers, providing design input and user feedback — to help optimize product design and implementation.

Client case study

Biovac Streamlines Pharmacovigilance with IQVIA Vigilance Platform​

Situation:
Biovac, a leader in South African healthcare, embarked on modernising its pharmacovigilance processes.

Challenge:
Biovac needed to transition from a labour-intensive, paper-based system to a digital solution to meet evolving regulatory standards and manage a large workload with a lean team.
Solution:
IQVIA was chosen for its AI capabilities and scalability, which aligned with Biovac's vision for future vaccine manufacturing. The partnership involved close collaboration and strategic planning, with a focus on improving efficiency and compliance.

Impact:
The implementation of IQVIA's technology resulted in substantial operational improvements at Biovac, significantly reducing time spent on data entry and enhancing compliance and quality control. This shift set a new benchmark in pharmacovigilance and paved the way for Biovac's future advancements in healthcare technology.

Comprehensive flexibility, integrated automation, and ensured effectiveness

  • The IQVIA Vigilance Platform offers complete coverage of all pharmacovigilance activities.
  • Real-time analytics allow comprehensive oversight and simplified aggregate reporting.
  • The SaaS platform enables seamless updates and compliance, with security and privacy management built in.
  • Near touchless handling of any format of incoming data and real-time quality and completion checking.
  • IQVIA’s globally distributed teams support organizations with local compliance.

 

Related solutions

Contact Us