

IQVIA.ai is a unified agentic AI platform specifically designed for life sciences that serves as the digital command center for how organizations operate, decide and innovate. By orchestrating tasks and insights across multiple data sources and functions, the platform helps organizations accelerate research and analysis, improve operational efficiency and support more confident, timely decision making.
Powered by IQVIA’s deep life sciences expertise, Healthcare-grade AI® and proprietary data – and enhanced by NVIDIA Nemotron and LangChain – IQVIA.ai actively learns from complex operational feedback while meeting your highest regulatory, privacy and quality standards.
Life sciences organizations face growing complexity. Data volumes are expanding, regulatory expectations are rising and teams are under pressure to deliver outcomes faster without compromising quality.
IQVIA.ai is designed to meet these challenges head‑on by helping organizations with intuitive, enterprise-ready capabilities to:
Explore the AI agents and MCP connectors powering IQVIA.ai – what’s available today and what’s coming next
Produce faster yet auditable evidence synthesis in line with accepted frameworks such as Cochrane by generating literature review output inclusive of search strategy and screened decisions from question, framework (e.g. PICO), and scientific literature sources
Available: Now
Save hours on multi-source deep research by receiving clear citation-backed research and reasoning with evidence-traceable synthesis in response to complex clinical or biomedical questions using IQVIA’s medical reasoning model, Med-R1
Available: Now
Produce faster regulatory guidance and accelerate requirement gathering by generating summaries of new or updated regulations from regulatory authorities and internal precedence
Available: Now
Generate fast, consistent patient analytics by building and maintaining high-quality clinical codelists from market details and inclusion/exclusion criteria
Available: Launch-Ready
Achieve faster and more consistent treatment or landscape insights by generating trial shortlists with extracted key characteristics and asset summary from indication and trial requirements
Available: Q1 '26
Increase quality, consistency, and comprehensiveness of clinical data review checks by automating setup, validation and lifecycle management directly from protocol requirements
Available: Q2 '26
Accelerate regulatory submissions and improve quality by generating master, country, and site Informed Consent Form (ICF) drafts from protocols, templates, and regulatory requirements
Available: Q2 '26
Drive higher compliance and quality with lower manual effort by automating the assessment, classification, validation and filing of Trial Master File (TMF) documents
Available: Q2 '26
Accelerate Clinical Study Report (CSR) delivery with increased quality and consistency by producing CSR drafts from the Statistical Analysis Plan (SAP), study protocol, and defined CSR templates
Available: Q3 '26
Gain higher data quality and improved protocol comprehension by delivering structured clinical trial protocol content extracted from protocol documents for fast analysis and reuse in downstream systems
Available: Q3 '26
Define market configuration, patient selection, physician mapping and reporting in minutes by automating end-to-end setup of healthcare alerts in the IQVIA Alerts Engine Platform using unstructured requirements and natural-language prompts
Available: Now
Improve planning and decision support and drive faster understanding for downstream processes by producing disease overview, standard of care (SoC), pathways and future landscape view from indication and pipeline context
Available: Launch-Ready
Produce faster cohort definition and patient counts for downstream analysis and workflows by creating and optionally executing patient cohorts from medical search terms and internal system code mapping engines
Available: Launch-Ready
Generate faster actionable insights for targeting and strategy by generating patient journey outputs and reporting dashboards from scoped requirements and cohort profiling
Available: Launch-Ready
Achieve faster and more precise targeting by automating detection of meaningful patient journey events and operationalizing them with timely outreach
Available: Launch-Ready
Plan and execute commercial campaigns with improved effectiveness by producing targeted go-to-market (GTM) and HCP engagement actions from brand performance, market analytics, syndicated and CRM signals
Available: Q2 '26
Generate insights and client recommendations in minutes by automating objective-based interview summaries, transcriptions, capture sheet with verbatim quotes, cross-interview analysis outputs, and subgroup analysis from interview audio recordings and project discussion guides
Available: Q2 '26
Achieve faster, more predictable survey completion and more efficient outreach and quota attainment by producing HCP opportunities with justification, email scheduling recommendations and near real-time monitoring from survey project parameters and HCP outreach history
Available: Q2 '26
Connects to diverse real‑world data sources to generate patient cohorts with flexible phenotyping and consistent definitions, enabling scalable population discovery to support clinical research, feasibility assessment, study design, and real‑world evidence generation
Available: Now
Connects to IQVIA’s syndicated global market intelligence, including MIDAS, Channel Dynamics and CD Verbatims, to provide data‑driven insights into market performance, demand drivers and commercial strategy across healthcare markets worldwide
Available: Now
Connects to continuously updated biomedical and healthcare literature enriched with ontologies to provide scalable evidence discovery and AI‑ready insights, supporting advanced research across life sciences, clinical development and medical affairs
Available: Now
Connects to practitioner and organization data from internal and external sources to provide a single trusted and compliant view, enabling consistent analytics, personalized engagement, and AI-driven decision‑making across commercial, medical and service teams
Available: Now
Connects to Trial Master File systems to provide secure, governed access to eTMF documents and metadata, enabling inspection readiness, audit context and compliant workflows with AI‑assisted retrieval, quality signals and automation without platform lock‑in
Available: Now
Connects to multiple clinical coding schemes to provide standardized creation and management of clinical codelists, enabling consistent definitions, reuse, and governance to support clinical research, analytics and real-world evidence workflows
Available: Coming Soon
Connects to clinical trial data sources to provide rapid identification, filtering and enrichment of trial information, enabling faster, more consistent pipeline, treatment-landscape and asset-level analysis for consulting and strategy workflows
Available: Coming Soon
Connects to internal and external healthcare data to identify, rank and rationalize drug analogues, enabling faster and more consistent forecasting, scenario analysis and strategic decision‑making across commercial, pipeline and due‑diligence workflows
Available: Coming Soon