IQVIA
Products: IQVIA Vigilance Platform, SmartSolve, MIDAS, Field Force Agent, OneKey, IQVIA NLP
IQVIA is a CRO and technology provider delivering clinical trials, real-world evidence, commercial intelligence and safety operations.
At a glance
Delivery model
Main areasCapabilities
IQVIA combines CRO services, real-world data and evidence, commercial intelligence, and safety and regulatory operations. Its portfolio also includes platforms and managed services for clinical data, engagement, quality, and compliance workflows.
Clinical Development
- Run clinical trials from protocol design and study start-up through patient enrollment and closeout with IQVIA’s full-service CRO services and clinical trial project management.
- Manage clinical data and trial execution with biometrics functional services, centralized data review, risk-based monitoring, eConsent, eCOA, IRT, site collaboration, and participant support.
Real-World Data and Evidence
- Plan and execute real-world evidence studies, including retrospective cohorts, prospective registries, pragmatic trials, external comparators, and post-authorization studies.
- Draw on IQVIA’s real-world data, including EMRs, claims, registries, and pharmacy records, and its analytics to support evidence generation, outcomes research, and payer or regulatory needs.
Commercial and Medical Affairs Execution
- Support commercial teams with IQVIA OneKey HCP/HCO reference data, IQVIA MIDAS global market intelligence, account planning, segmentation, targeting, call planning, omnichannel orchestration, and contract sales and outsourced field teams. IQVIA Field Force Agent is an AI assistant that helps field teams plan and execute compliant HCP engagements.
- Support medical affairs with IQVIA MSLs, AI-enabled medical information services, and medical insights from IQVIA NLP, which analyzes MSL notes and other sources to show what physicians and other stakeholders are discussing.
Safety, Regulatory and Quality Operations
- Outsource pharmacovigilance activities including adverse-event intake, ICSR case processing, local affiliate and QPPV services, safety analytics, signal management, and clinical trial safety operations. IQVIA Vigilance Platform supports safety-lifecycle workflows and data access.
- Manage regulatory and quality work with regulatory operations outsourcing, eCTD publishing, RIM platforms, regulatory intelligence, inspection readiness, GxP compliance consulting, computer system validation, and IQVIA SmartSolve for regulatory and quality workflows.
Best Fit
- Biopharma, medical device, and life-sciences teams seeking a CRO partner for clinical development, supported by biometrics, data, and trial technology services.
- Organizations that need coordinated real-world evidence, commercial intelligence, medical affairs, pharmacovigilance, regulatory, or quality capabilities across product development and commercialization.
Reviewed capability coverage
Backed by 56 pages from the vendor's own site. Select a capability to see its quote and source.
Clinical Development & Operations32 capabilities
CRO, Trial Management & Study Start-Up
Participant Recruitment, Retention & Decentralized Trials
Clinical Trial Systems, Data Capture & TMF
Trial Supply, Payments, Endpoints & Rater Services
Monitoring & Medical Oversight
Biostatistics & Statistical Methodology
Clinical Data Management & Database Programming
Biometrics FSP & Functional Services
PK/PD & Population Modeling
Clinical Pharmacology & Phase I Strategy
Exposure-Response, Dose Optimization & BA/BE
Clinical Development & Protocol Strategy
Feasibility & Site Strategy
Trial Budgeting & Forecasting
Medical Affairs, Evidence & Access42 capabilities
KOL, Medical Insights, Analytics & Advisory Boards
Medical Information & Field Medical
Medical Affairs Strategy, Operations & Integrated Evidence
Investigator Research, Grants, Publications & Scientific Communications
RWE Strategy, Protocols & Analytics
Epidemiology & Observational Research
Retrospective Studies, Chart Review & Registries
Post-Authorization Evidence & RWE Operations
Comparative Effectiveness & External Controls
HEOR, HTA & Outcomes Evidence
Market Access, Payer & Reimbursement Strategy
Value Communication, Coding & Field Access
Pricing, Contracting & Gross-to-Net
Market Access Intelligence, Platforms, Tender & Policy
Hub, Enrollment, Case Management & Contact Center
Reimbursement, Coverage & Field Access Support
Clinical Support, Adherence & Care Coordination
Data, Analytics & AI9 capabilities
Real-World & Reference Data
Data Integration, Interoperability & Warehousing
Master Data & Customer 360
Data Governance & Stewardship
Privacy-Preserving Data Linkage
Patient Journey & Population Analytics
Commercial Performance Measurement
Regulatory, Quality & Safety38 capabilities
PV Outsourcing, Governance & Compliance
Safety Technology, Reconciliation & Device Vigilance
Safety Intake, ICSR & Medical Review
Aggregate Reporting, Benefit-Risk & Risk Management
Literature, Signal & Clinical Trial Safety
Regulatory Writing, CMC, Labeling & Artwork
Regulatory Operations, Publishing & Information Management
Regulatory Strategy & Agency Interactions
Clinical & Marketing Applications
Device/IVD Regulatory Affairs & Regulatory Technology
QMS, CAPA, Change & Document Controls
GxP Compliance, Quality Risk & Product Quality
Audits, Supplier Quality & Inspection Readiness
CSV, Data Integrity & Process Validation
Healthcare Compliance Programs
Transparency & Aggregate Spend
Commercial & Customer Engagement17 capabilities
Contract Sales & Outsourced Field Teams
Territory, Roster & Incentive Operations
Account & Speaker Program Management
Market Research & Competitive Intelligence
Forecasting, Segmentation & Targeting
Brand & Market Strategy
CRM, Engagement Orchestration & Decisioning
Rep-Triggered Digital, eDetailing & Consent
Patient Engagement, Conversational AI & Virtual Events
Campaign Operations & Launch Activation
HCP, Patient & B2B Media / Marketing
Corporate Strategy & Enterprise4 capabilities
Product, Launch & Market Expansion Strategy
Corporate, Portfolio & Innovation Strategy
Translation, Corporate Communications & Investor Relations
Manufacturing & Supply Chain3 capabilities
Clinical Supply Planning, Procurement & Packaging
Specialty Pharma, CGT & Reverse Logistics
Human Factors, Verification & Reliability Testing
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