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.
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.
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.
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.
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.
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.
Take control of compliance and deliver seamless inspections with IQVIA eTMF
IQVIA Technologies has an electronic Trial Master File that simplifies today's over-engineered products and implementations, empowering oversight without busting the budget.
The IQVIA Electronic Trial Master File (eTMF) offers precision planning and intelligent automation to create and maintain an inspection-ready eTMF that you can count on. Its simple and intuitive design minimizes manual efforts and reduces risk.
Comparing eTMF solutions is complicated.
We can help.
IQVIA Technologies provides an RFI/RFP template that sponsors of all sizes have used to select and evaluate the features that mean the most to them.
Get actionable insights into quality, timeliness, and completeness in real-time
See your customized dashboards and metrics upon login to get immediate insights into eTMF health. Understand and correct quality, completeness, and timeliness issues proactively for nonstop audit-readiness
A practical approach to continuous eTMF compliance
IQVIA eTMF streamlines day-to-day TMF document workflows, quality control (QC) checks, and finalizations for your clinical operations. Guiding team members from task to task while maintaining detailed audit trails, IQVIA eTMF keeps everyone on the same page and always prepared for health authority inspections.
Study Set-Up Wizards
Quickly initiate new eTMF study environments with minimal clicks, guided by the eTMF study wizard.
Site Zone
Site-facing eTMF document exchange is simplified for site adoption with no additional integrations required.
eTMF Expert Services
IQVIA Technologies partners with your team and aligns resources to support eTMF document workflows, study-owner oversight, and eTMF DIA Reference Model quality assurance.
eTMF Archive
Remain inspection-ready beyond database lock and protect the huge investments made in completed trials. With simplified pricing independent of site volumes, IQVIA eTMF Archive drastically reduces the cost to comply with ICH GCP, FDA, and EMEA document retention requirements.
The IQVIA eTMF is part of a comprehensive suite of SaaS solutions that span the full trial continuum. We can support every aspect of trial design, start up, conduct, execution, and close out.