IQVIA functional services fills gaps and manages workflows with customized offerings to support a broad range of needs, including clinical data management, safety, regulatory, clinical monitoring, and biostatistics.
Specialized services, from statistical programming and medical writing, to deploying connected devices and the latest in advanced analytics, ensure the right resources are used at the right time. Benefits include
Our Models Include:
Whether you require resource management or a strategic outsourced centralized monitoring program, IQVIA’s clinical FSP programs provide a flexible mix of clinical monitoring expertise, resource management and technology-enabled solutions, each designed to deliver the results you need across your portfolio.
Our industry-leading centralized monitoring approach leverages IQVIA's global resource, real world data and advanced technologies to
Learn more about Clinical Monitoring.
IQVIA is using automation to create efficiencies – and reduce costs – for adverse event identification and reporting, translations, case processing and more. All backed by unparalleled global data, analytics and more than a dozen years of global FSP delivery excellence.
Depending on your organizational needs, IQVIA can deliver safety case processing, operational expertise or fully integrated safety services, processes and technologies.
Learn more about Pharmacovigilance.
Bring transparency, efficiency and predictability to your regulatory affairs strategy. IQVIA's flexible FSP programs let you outsource specific regulatory resources or configure fully integrated solutions.
A proprietary Regulatory Information Management (RIM) solution - IQVIA RIM Smart - powered by a centralized regulatory intelligence database and Business Process Management (BPM) tools support compliance and increase value for your product.
And with IQVIA's team of global regulatory scientists behind it all, you can manage regulatory challenges on a global scale, including
Learn more about Regulatory.
From building your database to locking it down, IQVIA's FSP resources provide customized, innovative data management solutions.
From full-time employee to outcomes-based projects, IQVIA's data management methods help you
And with interoperable, system agnostic platforms, you can adapt quickly to the changing clinical development landscape.
Learn more about Data Management.
Working from planning to outputs and reporting, our statistical programmers are experts in CDISC standards and provide the right level of expertise through a flexible and agile resourcing solution to ensure quality project deliverables.
Our experienced statistical programming teams are supported by experienced functional managers, allowing them to focus on high quality delivery of
Navigate the complexities of study design to drive speed and flexibility - without compromising quality. We help you turn data into actionable insights, reducing costs and risks, while accelerating timelines and quality of submissions.
Our biostatisticians use the latest technology and analytics to support all phases of clinical trials from trial design to publications. Our diverse trial design experience includes observational, real world evidence, adaptive, and complex Phase I design.
Our teams help reduce oversight time and ensure insightful interpretation through efficient production/QC of statistical components including
Learn more about Biostatistics.
Get an overview of IQVIA's full range of solutions to help you work more efficiently, standardize and improve controls across development stages and geographies.
Access non-identified patient data with IQVIA’s device-agnostic platform that can provide both real-time data and endpoints.
IQVIA FSP Advance integrates expert functional resourcing with clinical services and innovative technology solutions to increase quality and efficiency – within a clinical trial or across a global R&D portfolio.