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

DIGITAL TRIAL MANAGEMENT SUITE

CONTACT INFORMATION

IQVIA Technologies

4820 Emperor Blvd

Durham, NC 27703

UNITED STATES

Phone: 1-888-336-3748

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.