Utilize AI to analyze patient data, optimize therapeutic effectiveness, identify undiagnosed patients, and enhance engagement with healthcare professionals for improved patient outcomes.

Providing you with regulatory strategy, labeling, publishing, and intelligence solutions supported by our global expertise, data and technology, from early drug development through submissions and post-registration.

The key to your success is implementing automation, adopting advanced technologies, and leveraging insights from analytics that improve compliance and product safety. IQVIA provides flexible, innovative, scalable solutions to meet your unique business requirements.

IQVIA eTMF streamlines day-to-day TMF document workflows, quality control (QC) checks, and finalizations for your clinical operations.

Gain a deeper understanding of your patients and healthcare providers (HCPs) with IQVIA's AI-powered solutions and global patient data.

See why so many companies have standardized their clinical operations on the purpose-built, proven platform that gives sites the power to succeed and sponsors the insights they need to improve performance and compliance.

IQVIA’s Health Research Space platform is designed to meet the needs of real world direct-to-patient decentralized studies by providing an intuitive, all-in-one digital platform to support high-quality data collection and engagement with patients and / or their caregivers.

One Home for Sites is the only product that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a site needs to perform across all the clinical trials it is conducting.

Leverage real-time insights and advanced analytics to optimize brand strategies, enhance market adoption, and drive competitive advantage across global and local markets.

IQVIA Patient Experience Solutions with Apple devices - Introducing the next stage of innovation in patient engagement.

From grant submission to payment processing and closeout, IQVIA Grants and Funding Management empowers life sciences companies to effectively manage their strategic giving programs.

IQVIA’s Productivity Tools make authoring and PDF publishing easy, fast and efficient. And our validation tool ensures that what you submit is in technical compliance with health authority requirements.

IQVIA Human Assisted Review Tool (HART) combines human precision with industry-leading NLP.

Successfully address your most critical study design decision points with the IQVIA Planning Suite – driven by IQVIA Connected Intelligence™.

IQVIA Regulatory Intelligence provides real-time global regulatory updates, ensuring compliance and optimizing regulatory strategies.

CDAS (Clinical Data Analytics Solutions) is a vendor agnostic, flexible, modular, centralized data and analytics platform enabling your organization to execute trials, deploy data management, enable oversight, and/or run intelligent applications.

IQVIA ARK Patent Intelligence simplifies global patent navigation, aiding pharmaceutical innovation and strategic decision-making.

Simplify compliance in an age of growing complexity. Throughout the product lifecycle, IQVIA helps you manage quality compliance with a single enterprise software solution fit to serve your entire organization.

IQVIA Decentralized Trials deliver purpose-built clinical services and industry-leading technologies that engage the right patients wherever they are.

GrantPlan® simplifies the budgeting process, enabling life sciences companies and CROs to more efficiently, accurately and confidently build and adjust realistic clinical trial budgets and better negotiate investigator grants globally across all study phases and therapeutic areas.

IQVIA Oncology Commercial Solutions can help track the impact of clinical advancements in real world diagnosis and treatment patterns.

A successful launch strategy requires unprecedented data, advanced analytics, domain expertise and innovative technology. Gain the support you need from clinical development through post-launch optimization.

IQVIA Technologies' Clinical Trial Payments is a tech-enabled service offering, independent of IQVIA CRO services, that takes away the burden of making payments to sites around the world.

Fast, flexible and proven, IQVIA’s industry-leading electronic clinical outcome assessment (eCOA) platform ramps up efficiencies, delivers real-time data, and sharpens insights through best-in-class technology and a better patient experience.

Reach providers, patients, payers and key opinion leaders with relevant, timely, personalized communications that maximize commercial impact.

IQVIA’s Market Access Insights provides you with comprehensive, relevant, and actionable content so that you can make informed market access decisions.

Built on the Salesforce platform, HCP/O Engagement Management delivers a comprehensive solution for all touchpoints.

Harness decision intelligence and real-time insights with IQVIA Orchestrated Analytics (OA). Elevate your commercial strategy with advanced analytics and AI to master the dynamic market landscape.

Innovative gastroenterology and hepatology trials focus on advanced technology and evidence-based outcomes for effective therapies.

IQVIA Orchestrated Customer Engagement (OCE) embeds real-time intelligence into user workflows so commercial teams can personalize and optimize HCP engagements.

Innovative infectious disease trials accelerate vaccine development with real-time data and advanced analytics.

The IQVIA NLP Data Factory accurately surfaces and normalizes features of interest at scale to deliver comprehensive value across your organization.

The IQVIA NLP Insights Hub supports business users across the life sciences spectrum with analytics, insights and dashboards so you can focus on key organizational initiatives without spending valuable time gathering and sifting through information.

IQVIA SmartSolve eQMS for life sciences is an award-winning platform. It is your single source of truth to overcome regulatory challenges and manage the complexities of quality compliance.

IQVIA' s Expert Ecosystem provides a compliant, multi-dimensional and accurate view of scientific, clinical and digital expert leadership.

Streamline your regulatory processes with our new, end-to-end regulatory information management system, IQVIA RIM Smart. Free your team from labor-intensive maintenance to focus on delivering valuable products to market.

Innovative cell and gene therapies (CAGT) accelerate clinical development, offering life-changing treatments for patients worldwide.

IQVIA’s Analytic Research Accelerator provides a tailored solution for diverse cross-functional teams, with custom pricing strategies for unique business needs.

Comprehensive cardiovascular solutions enhance clinical trials, improving patient outcomes through innovative technologies and data-driven insights.

IQVIA Emerging Biopharma Analytics leverages data and expertise to guide critical business decisions in biopharma.

IQVIA Consumer Health gives you the connected intelligence you need to reveal fresh opportunities by bringing together our unparalleled data, advanced analytics, new technologies and cutting-edge services across the concept-to-consumer journey, so you are ready for the future of self-care.

Pediatric expertise is essential to developing and commercializing pediatric therapies, from the earliest planning stages through launch and real-world assessment.

IQVIA’s rare disease solutions enhance clinical trials, accelerating breakthroughs for over 350 million affected patients.

IQVIA Connected Intelligence integrates data, technology, and expertise to enhance decision-making and healthcare outcomes.

IQVIA MedTech accelerates innovation, enhancing healthcare outcomes through advanced technology and specialized solutions.

The IQVIA Patient Suite brings together best in breed products to save time and effort for sites and sponsors.

Delivering novel CNS (Central Nervous System) therapies is scientifically, medically and operationally complex. At IQVIA, we have more data and insights than ever before to drive innovation forward.

IQVIA NLP unlocks and transforms your data, at scale, from bench to bedside.

IQVIA NLP Interactive Extraction is our powerful NLP tool that unlocks your ability to process and structure the messy, hard-to-abstract textual data you need to support your business-critical decisions.

From data strategy to insights engines, and configurable to any data source, IQVIA’s Enterprise Information Management (EIM) suite of offerings and services provides the right foundation for you to become more data driven, agile and strategic.

Utilize AI-driven recommendations to deliver personalized, contextually relevant messages to healthcare professionals, enhancing engagement and optimizing omnichannel communication strategies.

The Health Technology Assessment (HTA) Accelerator from IQVIA lets you analyze past and current payer assessments and evidence requirements to guide clinical trial design and market access strategy across the product lifecycle.

IQVIA Value and Access (V&A) Strategy Consulting helps you define and defend product value across the entire lifecycle. Our customized solutions and proprietary tools support enhanced access to your treatments. 

AI-driven profiling enhances patient care by analyzing treatment patterns and improving healthcare provider engagement.

IQVIA Performance Management and Insights (PM&I) provide purpose-built life sciences BI solutions that support better decision-making for executives, multi-disciplinary brand and launch teams and field forces in all types and sizes of life science organizations.

Solutions available independent of IQVIA CRO services to increase efficiencies and site satisfaction across your trials.

IQVIA Consent is a comprehensive turnkey SaaS solution that aligns internal business and operational processes to easily comply with the growing number of data privacy laws around the globe, including GDPR and CCPA.

IRT (Interactive Response Technology). Cloud-based randomization and trial supply solution proven to reduce supply chain costs and improve study quality while accelerating study design, delivery and management

Discover how IQVIA Transparency Reporting reduces costs by simplifying data aggregation and reporting to help you maintain compliance across the globe.

The IQVIA Vigilance Platform is a drug safety system: a SaaS safety and pharmacovigilance platform that supports, streamlines, and enhances every phase of the safety lifecycle, driving down costs, improving quality and giving you easy access to your data.