Harness the power of global human expertise combined with automation, artificial intelligence (AI) and machine learning (ML) to design, build and execute end-to-end safety solutions.
IQVIA Vigilance Platform is our secure SaaS environment built to simplify safety and PV processes, while boosting speed, accuracy, and efficiency.
years of global and local experience
processed annually using artificial intelligence
words translated annually using intelligent automation in 11 languages
Meeting your compliance objectives in a world of constant change and financial challenges means doing things differently. It requires automating, adopting advanced technologies, and leveraging outsourcing.
Our innovative pharmacovigilance (PV) solutions are powered by the IQVIA Connected Intelligence -- integrated, scalable technologies combined with global data, advanced analytics, and deep domain expertise. Helping you predictably and cost-effectively achieve your safety and surveillance goals.
Gregg Dearhammer
SVP, Data Sciences, Safety and Medical (DSSM)
Technologies such as artificial intelligence (AI), machine learning (ML), and Natural Language Processing (NLP) are transforming today’s resource-intensive pharmacovigilance workloads, ensuring a more informed, more efficient approach.
Our end-to-end Local Affiliate Product Services (LAPS), with safety-focused industry experts and latest technologies, ensure global consistency at a local country level and compliance with all local safety requirements.
IQVIA's safety group also offers functional, operational and technical expertise in each geography, executed by integrated local teams that meet a range of time zone and language requirements. We handle hosting and safety management services via 16 validated, state of the art SSAE data centers designed with security, flexibility, scalability and vendor neutrality in mind.
Our pharmacovigilance business is one of the largest groups of PV experts worldwide, with a combination of deep life sciences expertise and best-in-class technologies. So you can expand your pharmacovigilance and safety capabilities with confidence - and without additional capital investment.
Leveraging AI and human expertise to strengthen local pharmacovigilance
How do we address barriers to improve drug availability?
Using AI in PV to enhance safety processes
Learn the latest developments across pharmacovigilance (PV), Medical Information (MI), and lifecycle management (LCM)
Unlock the secrets of Post-Approval LCM and LQPPV with IQVIA's expert white paper
Discover the evolution of pharmacovigilance operations, the rising trend of outsourcing, and the benefits of combined PV solutions.
An in-depth discussion on the impact of AI and regulatory changes on the pharmaceutical industry, with insights on the role of GenAI in drug development and pharmacovigilance, upcoming regulatory challenges, and the importance of integrating safety services with technology for future success.
New Solution Builds On Optical Character Recognition To Extract SAE Form Data
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Partner with compliance experts to create, implement and manage efficient, end-to-end processes that ensure your organization is compliant with global engagement and transparency regulations and codes.
Harness the power of global human expertise combined with automation, artificial intelligence (AI) and machine learning (ML) to design, build and execute end-to-end safety solutions.
Meet your regulatory needs using Real World Evidence to accelerate approvals and label expansions in the U.S. and EU.
Scale drug safety and pharmacovigilance across geographies and languages
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