Drug Safety and Pharmacovigilance
Harness the power of automation to execute streamlined end-to-end safety solutions while reducing costs.
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Americas
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Asia & Oceania
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Regions
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Americas
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Asia & Oceania
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Europe
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Middle East & Africa
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Americas
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Asia & Oceania
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Europe
Europe
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
SOLUTIONS
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Research & Development
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Real World Evidence
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Commercialization
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Safety & Regulatory Compliance
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Technologies
LIFE SCIENCE SEGMENTS
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THERAPEUTIC AREAS
- Cardiovascular
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- Oncology
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Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
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IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
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Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm. IQVIA and Apple are collaborating to bring this exciting future of personalized care directly to devices patients already have and use.
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SEARCH JOBSWhite Paper
The Future of Safety
How automation and machine learning are transforming Pharmacovigilance
Mar 28, 2019
Introduction
Despite rapid advances in technology, pharmacovigilance (PV) units still handle the majority of adverse event and safety information data collection and processing through manual efforts. Once the data is captured, it is often stored in siloed databases making it difficult if not impossible to aggregate and analyze in meaningful ways.
According to the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA), the amount of adverse event reporting is increasing by more than 15 percent annually. Adding to this complexity, the number and variety of data sources PV units are expected to review is growing exponentially, making it increasingly difficult for PV professionals to keep up.
Many of these data sources are unstructured in nature where information has to be culled from narratives rather than directly lifted from forms and reports. These unstructured sources include emails, social media posts, journal articles, audio files, and handwritten documents, some of which require language translation prior to extracting relevant details.
The deluge of new data, increasing requirements from regulators, and declining PV budgets are forcing the PV community to seek new solutions to improve the access, timeliness and cost-effectiveness of safety data management.
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Related solutions
Safety & Regulatory Compliance
Meet the challenge of changing stakeholder demands and increasing cost constraints with IQVIA's integrated technology services and analytics-driven offerings.