With over 4,000 professionals worldwide and over 600 country-based staff, IQVIA’s robust safety organization can provide end-to-end solutions with regulatory-focused medical experts and leading technologies to support your local safety needs.
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. From single country, regional, to full international support, the IQVIA LAPS model allows customers to build a strategy that fits their needs while driving operational and budgetary efficiencies.
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.
End-to-end solutions with regulatory-focused medical experts and leading technologies to support your local safety needs and drive consistency with global requirements
At the local affiliate level, maintaining compliant PV and MI models entails a wide variety of requisites
Medical Information organizations are redefining how people and AI can work together to rapidly respond to the surge in customer requests.
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.
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.
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