PUBLISHER: Prescient & Strategic Intelligence | PRODUCT CODE: 1635118
PUBLISHER: Prescient & Strategic Intelligence | PRODUCT CODE: 1635118
The global pharmacovigilance market is projected to grow from $8,340.1 million in 2024 to $18,026.7 million by 2030, reflecting a compound annual growth rate (CAGR) of 13.9% during the forecast period.
This growth is driven by the increasing incidence of adverse drug reactions (ADRs) and a heightened emphasis on drug safety and efficacy. The rising prevalence of chronic diseases necessitates the development of new pharmaceuticals, further underscoring the importance of robust pharmacovigilance systems to monitor and manage potential drug-related risks.
Key Insights
The Phase IV (post-marketing) segment holds a significant share in the pharmacovigilance market, as continuous monitoring of drug safety after market approval is crucial for detecting rare or long-term adverse effects.
Pharmaceutical companies are the largest end-users of pharmacovigilance services, investing heavily in monitoring the safety profiles of their products to comply with stringent regulatory requirements and maintain public trust.
The spontaneous reporting segment is expected to witness substantial growth, driven by the increasing adoption of this method for its efficiency in detecting new, rare, and serious ADRs.
North America leads the pharmacovigilance market, attributed to advanced healthcare infrastructure, a high incidence of chronic diseases, and stringent regulatory policies enforcing drug safety monitoring.
The Asia-Pacific region is anticipated to experience the fastest growth during the forecast period, propelled by increasing clinical trial activities, rising healthcare expenditure, and growing awareness of drug safety among healthcare professionals and patients.
The integration of artificial intelligence (AI) and machine learning (ML) technologies in pharmacovigilance processes is enhancing the efficiency and accuracy of ADR detection, analysis, and prediction, driving market growth.
The outsourcing of pharmacovigilance services to contract research organizations (CROs) is becoming increasingly prevalent, allowing pharmaceutical companies to focus on core activities while ensuring comprehensive drug safety monitoring.
The growing emphasis on personalized medicine necessitates more complex pharmacovigilance techniques to monitor side effects and long-term consequences tailored to individual genetic profiles, influencing market dynamics.