The AI in
pharmacovigilance market is expected to grow at a CAGR of
12–15% from 2023 to 2030, driven by the need to automate adverse
event data processing, stringent regulatory requirements, advancements in AI
analytics, cost reduction benefits, and the increasing use of real-world
evidence. These factors reshape pharmacovigilance processes, ensuring faster
and more accurate safety assessments. However, high implementation costs and
data privacy concerns pose challenges to the market growth.
Artificial intelligence (AI) in pharmacovigilance refers to
applying machine learning, natural language processing, and other AI
technologies to enhance the monitoring, detection, assessment, and prevention
of adverse drug reactions and related issues. It helps streamline the
traditionally manual processes involved in pharmacovigilance by automating data
extraction, signal detection, and case processing. AI facilitates faster and
more accurate analysis of large datasets, ensuring regulatory compliance and improving
drug safety. The technology is particularly valuable in managing the
complexities of real-world data, including unstructured information from
medical records, social media, and adverse event reports.
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Growing Volume of Adverse Event Data
The increasing volume and complexity of adverse drug
reaction (ADR) data are major factors driving the adoption of AI in
pharmacovigilance. With the rise of global drug usage and access to various
reporting channels, pharmacovigilance teams are overwhelmed by the sheer amount
of structured and unstructured data generated daily. AI technologies, such as
machine learning and natural language processing, enable efficient data
extraction, deduplication, and classification from disparate sources, such as
electronic health records, social media, and clinical trial databases.
Automating these processes reduces human errors and ensures faster
identification of potential safety signals, allowing quicker interventions.
This capability is especially crucial as pharmaceutical companies face
stringent timelines to comply with regulatory requirements and ensure public
safety. By leveraging AI, the industry can handle data growth while maintaining
cost efficiency and precision.
Integration of AI with Real-World Data Analytics
One significant advancement boosting the market is the
integration of AI with real-world data (RWD) analytics in pharmacovigilance.
RWD, sourced from electronic medical records, wearable devices, and patient
registries, offers valuable insights into drug safety and efficacy in real-life
settings. AI-powered algorithms can process and analyze these vast datasets to
detect adverse drug reactions and patterns that might go unnoticed in clinical
trials. Additionally, AI enables the identification of rare or long-term side
effects through predictive modeling and signal detection. This integration
enhances proactive safety monitoring, improves decision-making, and aids in
personalized medicine approaches. As regulators increasingly recognize the
importance of RWD in drug safety evaluations, the use of AI-driven RWD
analytics has become a transformative force in the pharmacovigilance landscape,
offering faster and more accurate results to safeguard patient health.
Competitive Landscape Analysis
The global AI in pharmacovigilance market is marked by the
presence of established and emerging market players such as WNS, Accenture
Plc, IQVIA Inc, Oracle, PAREXEL International
Corporation, Cognizant and Aris Global among others.
Some of the key strategies adopted by market players include new product
development, strategic partnerships and collaborations, and geographic
expansion.
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insights
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Global AI in Pharmacovigilance Market
Segmentation
This report by Medi-Tech Insights provides the size of
the global AI in pharmacovigilance market at the regional- and
country-level from 2023 to 2030. The report further segments the market based
on component, deployment and end-user.
- Market
Size & Forecast (2023-2030), By Component, USD Million
- Software
- Services
- Market
Size & Forecast (2023-2030), By Deployment, USD Million
- On-premises
- Cloud-based
- Market
Size & Forecast (2023-2030), By End-user, USD Million
- Pharmaceutical
and Biotech Companies
- Contract
Research Organizations (CROs)
- Others
- Market
Size & Forecast (2023-2030), By Region, USD Million
- North
America
- US
- Canada
- Europe
- UK
- Germany
- Italy
- Spain
- Rest
of Europe
- Asia
Pacific
- China
- India
- Japan
- Rest
of Asia Pacific
- Latin
America
- Middle
East & Africa
About Medi-Tech Insights
Medi-Tech Insights is a healthcare-focused business research
& insights firm. Our clients include Fortune 500 companies, blue-chip
investors & hyper-growth start-ups. We have completed 100+ projects in
Digital Health, Healthcare IT, Medical Technology, Medical Devices & Pharma
Services in the areas of market assessments, due diligence, competitive
intelligence, market sizing and forecasting, pricing analysis &
go-to-market strategy. Our methodology includes rigorous secondary research combined
with deep-dive interviews with industry-leading CXO, VPs, and key demand/supply
side decision-makers.
Contact:
Ruta Halde
Associate, Medi-Tech Insights
+32 498 86 80 79
info@meditechinsights.com

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