IQVIA's safety teams harness the power of automation, artificial intelligence (AI) and machine learning (ML) to design, build, and execute end-to-end safety solutions.
And as one of the world's largest pharmacovigilance organizations, IQVIA brings extensive domain expertise and deep regulatory intelligence to your program.
IQVIA is leading the charge in leveraging artificial intelligence and smart machines to identify, ingest, and report out safety signals in structured and unstructured data.
ANNETTE WILLIAMS, R.PH, VP, PHARMACOVIGILANCE, IQVIA
New Solution Builds On Optical Character Recognition To Extract SAE Form Data
Establishing an endpoint adjudication committee and key endpoint management strategy
At the local affiliate level, maintaining compliant PV and MI models entails a wide variety of requisites
Beyond meeting compliance standards, pharmaceutical companies must implement the quality systems necessary to handle data in the local language, ensure data privacy, and minimize risk.
Delivering a unique blend of innovation, technical expertise, and adaptative strategies, IQVIA CEVA was able to overcome tight timelines and meet client targets for their COVID-19 therapeutic trial
IQVIA's Safety and Aggregate Reporting Center
Using artificial intelligence and smart machines for scalability and cost effectiveness
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. Expand your pharmacovigilance, Medical Information, and safety capabilities with confidence - and without additional capital investment.
In an increasingly self-serve, digital-first world, compliantly boost speed, accuracy, flexibility and coverage with AI-powered IQVIA Medical Information services
The CEVA group is a dedicated department within IQVIA that specializes in the compilation and management of study committees. CEVA endpoint adjudication pillar supports committees that need to review additional data related to a specific event, timepoint, lab result etc. that needs to be gathered from sites or external vendors and this group primarily supports endpoint adjudication committees.
.svg){kind=icon}
