ABOUT IQVIA TECHNOLOGIES
IQVIA Technologies develops purpose-built solutions on a future-state architecture to enable connected intelligence across the entire life sciences product lifecycle. Under our Orchestrated Clinical Trials (OCT) platform, we’re driving smarter, faster trials for sponsors, sites and patients, with more than 20 market-leading, cloud-based products and tech-enabled services. These best-of-breed technologies are grouped as Digital Suites and are available independently of our CRO services, with support models customized to meet your specific business needs.
DIGITAL PATIENT SUITE
Biosample collection is an inevitable part of most clinical trials. Learn how sponsors should be tracking every sample back to the source so as to not violate compliance issues.
Master protocol design trials require an endless stream of consent forms, which add time, cost, and risk. A feature-rich electronic consent platform can simplify those processes and improve patient engagement.
Electronic consent products set the stage for a better trial experience for all stakeholders, but many sites and sponsors are wary of giving up their paper-based past.
IQVIA Complete Consent provides an easy, secure way to deliver highly engaging, regulatory compliant electronic consent for trials of all types.
DIGITAL TRIAL MANAGEMENT SUITE
Examine six of the more significant points from the draft guidance, specifically as they pertain to the electronic Trial Master File.
Delve into how an intelligent eTMF application is an example of an in-production capability enhanced by artificial intelligence and used by over 6,000 employees across the globe in multiple languages.
While an eTMF can be custom-configured upfront to meet the specific demands of a study, discover how IQVIA’s eTMF delivers the most advanced and sophisticated features and functionality available today.
Securely Archive, Lock Down, Provide Access, & Ensure Compliance Of Your Electronic Trial Master File
Trying to archive a TMF delivered by a CRO partner? Looking to move out of non-compliant file systems? Interested in reducing the high costs of archiving an active eTMF? Discover how IQVIA™ eArchive could be the solution for these issues and more.
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Contact: Turquiose Ross, MBA
DIGITAL PLANNING SUITE
Building an accurate budget for a clinical trial comes with a host of challenges. These include, but are not limited to, intricate protocols, large enrollments, shortened timelines and global sites. By using a benchmarking tool that uses a global dataset experts can develop Fair market Value (FMV) costs.
DIGITAL SITE SUITE
Understand why companies have standardized their operations on the purpose-built, proven platform that gives sites the power to succeed and sponsors the insights to improve performance and compliance.
In clinical research, staffing shortages can delay trials and prevent new therapies from getting to patients in need. Read why Melissa Easy, VP, Clinical Technologies at IQVIA, believes advanced tech may bridge this gap as she reviews tools that are proving useful to study teams.
The European Union Clinical Trial Regulation No. 536/2014 recently introduced the most significant changes to the processes for clinical trial applications in at least the past 15 years. Learn how this impacts the Trial Master File and consider three key functions that an electronic TMF must have to achieve compliance and maintain organizational success.
Learn how the IQVIA Investigator Site Portal reduces activation timelines and eliminates site frustrations by automating processes and providing complete oversight to study teams.