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
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
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.
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
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.
Navigate the complexities of study design to arrive at insights that drive speed and flexibility - without compromising quality.
IQVIA's seasoned biostatisticians turn data into actionable insights, fueling clinical trial success by reducing costs and risks, and accelerating timelines and quality of submissions.
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.