Patient Recruitment
Predict enrollment more accurately and increase the number of patients per site using data-driven patient recruitment solutions.
-
Americas
-
Asia & Oceania
-
A-I
J-Z
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Regions
-
Americas
-
Asia & Oceania
-
Europe
-
Middle East & Africa
-
Americas
-
Asia & Oceania
-
Europe
Europe
- Adriatic
- Belgium
- Bulgaria
- Czech Republic
- Deutschland
- España
- France
- Greece
- Hungary
- Ireland
- Israel
- Italia
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
SOLUTIONS
-
Research & Development
-
Real World Evidence
-
Commercialization
-
Safety & Regulatory Compliance
-
Technologies
-
Patient Engagement
LIFE SCIENCE SEGMENTS
HEALTHCARE SEGMENTS
- Information Partner Services
- Financial Institutions
- Public Health and Government
- Patient Associations
- Payers
- Providers
THERAPEUTIC AREAS
- Cardiovascular
- Cell and Gene Therapy
- Central Nervous System
- GI & Hepatology
- Infectious Diseases and Vaccines
- Oncology
- Pediatrics
- Rare Diseases
- View All
Impacting People's Lives
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
LEARN MORE
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.
Research & Development OverviewResearch & Development Quick Links
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.
REAL WORLD EVIDENCE OVERVIEWReal World Evidence Quick Links
See markets more clearly. Opportunities more often.
Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
COMMERCIALIZATION OVERVIEWCommercialization Quick Links
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.
COMPLIANCE OVERVIEWSafety & Regulatory Compliance Quick Links
Intelligence that transforms life sciences end-to-end.
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWTechnology Quick Links
Advance your patient engagement strategy
Discover new patient engagement possibilities with IQVIA insights, expertise, and technology-driven solutions.
Patient Engagement OverviewPatient Engagement Quick Links
- Commercial Engagement Solutions
- Commercial Patient Engagement Suite
- eCOA
- Clinical Outcome Assessment (COA) instrument library
- Linguistic Validation
- Patient-Centered Endpoints
- Engagement Services (US)
- Association Management
- Recruitment
- Journey Analytics
- Patient Finder
- Disease insights
- Disease Registries
- Treatment satisfaction
CLINICAL PRODUCTS
COMMERCIAL PRODUCTS
COMPLIANCE, SAFETY, REG PRODUCTS
BLOGS, WHITE PAPERS & CASE STUDIES
Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSTHE IQVIA INSTITUTE
An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
SEE LATEST REPORTSFEATURED INNOVATIONS
-
IQVIA Connected Intelligence™
-
IQVIA Healthcare-grade AI™
-
Human Data Science Cloud
-
IQVIA Innovation Hub
-
Decentralized Trials
-
Patient Experience powered by Apple
WHO WE ARE
- Our Story
- Our Impact
- Commitment to Public Health
- Code of Conduct
- Environmental Social Governance
- Privacy
- Executive Team
NEWS & RESOURCES
Unlock your potential to drive healthcare forward
By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
LEARN MORE
IQVIA AI is Healthcare-grade AI
Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.
LEARN MORE
Your healthcare data deserves more than just a cloud.
The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.
LEARN MORE
Innovations make an impact when bold ideas meet powerful partnerships
The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.
LEARN MORE
Proven, faster DCT solutions
IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
LEARN MORE
IQVIA Patient Experience Solutions powered by Apple
Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm. IQVIA and Apple are collaborating to bring this exciting future of personalized care directly to devices patients already have and use.
LEARN MOREWORKING AT IQVIA
Our mission is to accelerate innovation for a healthier world. Together, we can solve customer challenges and improve patient lives.
LEARN MORELIFE AT IQVIA
Careers, culture and everything in between. Find out what’s going on right here, right now.
LEARN MORE
WE’RE HIRING
"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.
SEARCH JOBSBlog
Why and How is Clinical Monitoring Transforming at Speed – Are you ready for the future?
The global pandemic: a catalyst for long overdue changes in clinical trial monitoring?
Jun 02, 2021
The global pandemic created challenges the healthcare industry never could have imagined. However, it also opened the doors to innovation in trial conduct. For an industry that is cautious and modest in change, the pandemic accelerated the pace of innovation, adopting virtual technologies and digitization of processes in clinical research like never before.
One specific change is the adoption and rapid inclusion of remote and centralized monitoring and advanced analytics in lieu of more traditional on-site approaches. This change requires a level of expertise and experience that sponsors may not hold in-house and may consider use of a functional service provider, or FSP, to manage.
For more than a decade, regulatory bodies and other industry stakeholders have weighed in on the use of risk-based monitoring (RBM). The U.S. Food and Drug Administration and European Medicines Agency have provided guidance encouraging the use of centralized monitoring methods when appropriate.
Despite regulatory support, adoption of these models was slower than anticipated prior to the pandemic. However, we have witnessed tremendous advances in new clinical trial designs and technologies to mitigate against longstanding challenges to drug development.
Given lessons learned during the pandemic, sponsors may consider integrating technology and analytics across their portfolios moving forward, and how FSP experts may be able to help accomplish this.
Modernizing monitoring
Technology enablement is key to transforming trial monitoring in several ways, including automated key risk indicator (KRI) management, early signal detection across patient safety and eligibility, and fully auditable and traceable workflows to manage risks at the study, site and patient level.
If looking at modernizing monitoring in incremental levels, sponsors could see integration as:- Level 1: Delivering RBM through risk-based strategies and centralized monitoring where use of analytics and automated processes can reduce source verification of data and effort for clinical research associates (CRAs) normally associated with on-site monitoring visits.
- Level 2: Connecting RBM and decentralized trials (DCT) by utilizing integrated monitoring capabilities and emerging DCT technology framework to enable remote patient and site management while removing onsite-specific tasks, allowing for more time and focus for patient needs.
- Level 3: Using patient-generated data via remote monitoring data collection to further transform clinical monitoring and enhance direct-to-patient tools and processes.
IQVIA’s FSP tech-enabled capabilities and breadth of data integration and analytics services allow sponsors to build a successful journey mapping through these three levels of operating model transformation. Implementation of decentralized and direct-to-patient process elements is driving demonstrable benefits in meeting patient recruitment needs for clinical research. In addition, the use of artificial intelligence and machine learning (AI/ML) capabilities enable monitoring of safety trends across sites, participants, or regions to make needed changes quickly.
Integrated technologies
In order to make the shift to remotely-managed sites, sponsors must ensure needed information is available and accessible remotely. Key components to ensure data integration improves downstream processes and does not increase patient and site burdens, include: Trial design and process: simplified protocols and fit-for-purpose electronic data capture (EDC) design.- New technology: IQVIA uses a Central Data Repository or CDR to hold information from various trial stages through use of technologies, including IQVIA’s decentralized trial platform, connected devices, electronic consent (eConsent) and more.
Data-driven integrated processes: Enabling integration of data-driven processes across trial activities can help ensure meaningful insights are not siloed but rather maximized to elevate data quality and patient safety.
Understanding the benefits
Regardless of the changing clinical development landscape, the one constant for all industry stakeholders is prioritizing patient safety and improving patient outcomes, where data quality plays a key role. As sponsors consider modern approaches to monitoring, understanding the “why” of changing their approach matters. Several key benefits to RBM and centralized monitoring, include:- Real-time visibility and automated identification of
- monitoring insights to make adjustments quickly.
- opportunities to proactively investigate to reduce the proliferation of potential errors or instances of non-compliance with the protocol.
- Early signal detection and subject-level data review
- helps to achieve high data quality and integrity, thus avoiding end-of-study delays.
- Automating processes to drive faster actions can:
- accelerate data availability for reporting study results,
- reduce overall timelines to potentially get therapies to market faster.
In addition to clinical monitoring improvements, these methods can lower the total cost of clinical monitoring for a clinical trial by as much as 40%, and when adopted at scale across an enterprise, generate opportunity to invest those savings in more clinical research.
We now have a tangible example of how adversity can inspire innovation. If you wish to capitalize on the momentum for change and transform your clinical trial monitoring approaches, learn and co-discover with our experts as they share insights from more than a decade of experience in executing risk-based approaches to clinical trial monitoring across a full spectrum of outsourcing solutions (Staff Augmentation, FSP Outsourced, FSP Advance, End-to-End Full Service Delivery).
Please contact us directly to learn more about FSP capabilities and other outsourcing solutions specific to centralized monitoring or please visit globalFSPGTM@iqvia.com.
Related solutions
Clinical Trials
Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.
Functional Services
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Clinical Research & Development Solutions
Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.