Therapeutic and Specialty Centers of Excellence offer scientific expertise, therapeutic insights and clinical trial experience to expedite new therapies for patients.
Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
Real World Evidence. Real Confidence. Real Results.
Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
Service driven. Tech-enabled. Integrated compliance.
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
IQVIA Technologies helps life sciences accelerate innovation to make a greater impact on human health. Our transformative technologies harness intelligence, integrate industry leading data and analytics, and use advanced AI/ML capabilities to unleash business potential faster.
At IQVIA our foundation is built on innovation. We are committed to finding new and smarter approaches to solving customer challenges. Explore some of the latest ways we can help drive your results.
Therapeutic and Specialty Centers of Excellence offer scientific expertise, therapeutic insights and clinical trial experience to expedite new therapies for patients.
Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
Real World Evidence. Real Confidence. Real Results.
Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
Service driven. Tech-enabled. Integrated compliance.
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
IQVIA Technologies helps life sciences accelerate innovation to make a greater impact on human health. Our transformative technologies harness intelligence, integrate industry leading data and analytics, and use advanced AI/ML capabilities to unleash business potential faster.
At IQVIA our foundation is built on innovation. We are committed to finding new and smarter approaches to solving customer challenges. Explore some of the latest ways we can help drive your results.
Experts in the science of measuring patient outcomes
The measurement of patient experience is a science. Collecting valid patient experience data (PED) helps support regulatory approvals and reimbursement, and promotes market access and product differentiation. But the first challenge in PED is determining what data to capture—and the right way to capture that data—in order to draw valuable insights directly from the patient while complying with regulatory guidelines.
IQVIA’s Patient Centered Solutions (PCS) team is a global leader in the science of measuring meaningful patient outcomes. PCS applies scientific discipline to accurately capture the patient experience and incorporate PED into trial endpoints primarily through the use of standardized questionnaires or instruments known as clinical outcome assessments (COAs).
By enriching study processes with patient-centricity, we help leading biopharma companies define smarter endpoints, gain market access and earn distinction in crowded categories.
Patient-reported outcome (PRO)
Observer-reported outcome (ObsRO)
Clinician-reported outcome (ClinRO)
Performance outcome (PerfO)
Disease-related signs and symptoms
Treatment-related symptoms
Impacts of disease and treatment
Health-related quality of life (HRQoL)
Patient preferences and priorities
Digital health data
The complete patient experience data solution
Only IQVIA offers a fully integrated, global PED solution—combining strategy and outcomes research, instrument licensing and development, expert COA design and implementation services, and clinical rater services (formerly Cronos Clinical Consulting). We partner with you from start to finish to simplify handoffs, embed regulatory expertise, and enable faster, more precise execution.
INTEGRATED APPROACH
IQVIA’s end-to-end PED workflow
The PCS team is relentlessly focused on advancing science and technologies for capturing, benchmarking and interpreting actionable data from the patient’s perspective. We support quality PED collection and COA strategy from clinical implementation to data analysis, interpretation and dissemination.
Setting the standard in patient experience data
Strategic PED consulting and outcomes research
IQVIA leads early-stage PED strategy, defining what to measure and how, applying scientific and therapeutic expertise, especially in CNS and oncology conditions. We develop study design, outcomes research, real-world evidence (RWE) generation, COA implementation, regulatory endpoint consulting and stakeholder alignment to prioritize the right measures for approvals and reimbursement. As the leader in PED services, the IQVIA PCS team guides the industry in strategically identifying what matters to most to patients.
We provide on-demand access to linguistically validated COAs, standardized scoring, benchmarking, and custom instrument development across languages and regions. IQVIA focuses on providing our customers with reliable, valid measurement tools across the broadest range of therapeutic areas and geographies to make instrument licensing simple, fast and easy. If your preferred instrument isn’t available in our COA Marketplace, we’ll manage the licensing process on your behalf, ensuring quick and seamless acquisition regardless of ownership.
With a commitment to amplifying the patient voice in clinical research, IQVIA has assembled a robust collection of clinical outcome assessments in our intuitive, easy-to-access COA Marketplace. Explore 100+ proven and respected instruments available to license for use in a wide range of healthcare-related outcomes.
IQVIA delivers expert COA design and implementation, integration of electronic clinical outcome assessment (eCOA) solutions, rater training and rater oversight (formerly Cronos Clinical Consulting) and intervention services based on a proprietary risk-based data monitoring (RBDM) platform. We support successful translation from protocol design to implementation of COAs in global research studies to ensure data quality and study integrity.
Our book Patient-centricity in the Biopharmaceutical Industry: Are We Nearly There Yet? gathers insights on patient-centric intervention development from a diverse group of more than 30 experts.
Using Patient Experience Data to Evaluate Medical Interventions collects thoughtful perspectives from physicians, medical researchers, social scientists and strategy consultants.
Defining and Analyzing Patient-centric Endpoints Based on COAs and Digital Technologies promotes the basics of COA implementation and analysis in the pharma industry.
The right endpoint strategy is just the beginning
Forward-thinking biopharma companies are more engaged with the science of meaningful change in patient health. We bring together the expertise in the patient science, the know-how for studies, the understanding of patient preference, and the intellectual IP of how instruments work.
Our approach minimizes the impact of handoffs from one stage to the next, enabling you to go faster with greater efficiency and demonstrate ROI from PED.
Scientifically rigorous, easily interpretable and actionable patient experience data (PED) can help researchers and clinicians make pivotal decisions during the development and commercialization of interventions.
Marie E. Lamont
VP, Global Head of Patient Insights, Experience and Registry Solutions, Real World Solutions
Elan Josielewski
Senior Director, Patient Centered Solutions and General Manager, IQVIA Quality Metric
Matthew Reaney, PhD
Global Science & Analytics Lead, IQVIA PCS, Head of the PCS Institute
PCS Frequently Asked Questions (FAQs)
Learn more about Patient Centered Solutions
Patient experience data (PED) is information that captures patients’ experiences, perspectives, needs, and priorities related (but not limited) to disease symptoms, disease impacts, treatment burden, preferences, and disease burden. PED enables you to understand and study the right population, assessing the right endpoints and collect the right data which inform the right messages to deliver the right outcomes to communicate true product value beyond advances in survival.
Patient experience data (PED) is collected using structured and scientifically validated methods that capture how patients feel, function, and experience disease and treatment during clinical research and beyond. The types of studies that collect PED include clinical, qualitative, observational survey, patient preference, natural history, and mixed method studies.
Clinical outcome assessments (COAs) are a measure that describes or reflects how a patient feels, functions, or survives. COAs are standardized questionnaires, sometimes called instruments, that are used to measure outcomes related to the patient experience and incorporate PED into trial endpoints.
COAs can be:
Patient-reported outcomes (PRO)
Observer-reported outcomes (ObsRO)
Clinician-reported outcomes (ClinRO)
Performance outcomes (PerfO)
COAs are commonly used to measure outcomes such as disease-related signs and symptoms, treatment-related symptoms, impacts of disease and treatment, health-related quality of life (HRQoL), patient preferences and priorities, and digital health data.
An integrated PED solution connects services across the lifecycle, combining strategy and outcomes research, instrument licensing and development, COA design and implementation, and clinical rater services to simplify handoffs and support faster, more precise execution.
Strategic PED consulting includes early-stage work defining what to measure and how to measure it. The work includes study design, outcomes research, real-world evidence (RWE) generation, COA implementation, regulatory endpoint consulting, and stakeholder alignment to prioritize measures for approvals and reimbursement.
The IQVIA COA Marketplace is an online library that provides access to validated clinical outcome assessments (COAs) that can be licensed and used in clinical trials, real‑world studies, and healthcare research. It brings together a large portfolio of scientifically validated instruments in one place to help researchers identify, evaluate, and license fit‑for‑purpose measures efficiently.
Yes, if a preferred COA instrument isn’t available in IQVIA’s COA Marketplace, IQVIA can manage the licensing process on your behalf, supporting acquisition regardless of ownership.
IQVIA’s licensing information describes full-service licensing, distribution, and translation/linguistic validation, including support even when the copyright holder is not IQVIA, helping ensure correct versions/permissions and validated translations.
In-trial interviews can be used to generate early insights on patient experience with new treatments, help assess patient relevance of novel endpoints, and improve trial design. They can identify qualitative insights on treatment experience, side effects/tolerability, ease of use, and support COA validation and protocol understanding.
Clinical rater services include rater training and calibration, ongoing rater oversight and intervention, independent and centralized ratings, eligibility confirmation, remote and telehealth-enabled assessments, and patient engagement support.
Partner with IQVIA’s Patient Centered Solutions team to execute a more precise PED strategy that meets global regulatory requirements, delivers relevant product differentiation, and applies patient insights for optimal outcomes.