Decrease clinical development costs and increase study quality using our global functional resources
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Clinical Monitoring
Data Management
Statistical Programming
Biostatistics
Medical Writing
Lifecycle Safety
Regulatory Affairs
Biostatistics
Make analytics a competitive advantage
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.
Data Management
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
• Engage patients
• Improve data transparency
• Ensure data quality
• Allow for early problem solving
• Reduce oversight time
And with interoperable, system agnostic platforms, you can adapt quickly to the changing clinical development landscape.
Lifecycle Safety
Manage safety across the product lifecycle
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 15 years of global FSP delivery excellence.
Statistical Programming
Drive automation to reduce cycle times
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.
Medical Writing
Clarity and transparency in regulatory documents
Create transparency in your regulatory documents with a range of medical writing services that deliver quality and timeliness throughout your product development lifecycle.
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Clinical Monitoring
From resource management to centralized monitoring
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 enhance patient safety and improve data quality.
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Regulatory Affairs
Stay a step ahead of change
Navigate complete regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
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Clinical Monitoring
Data Management
Statistical Programming
Biostatistics
Medical Writing
Lifecycle Safety
Regulatory Affairs
Statistical Programming
Medical Writing
Lifecycle Safety
Data Management
Biostatistics
Clinical Monitoring
Regulatory Affairs
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section to
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Trial Management
Trial Management
Trial Management
Trial Management
Driving value by innovating the way you manage trials
IQVIA's FSP programs successfully deliver various functional trial management solutions, identifying and staffing key leadership roles with global project management experience. We provide a flexible and dedicated workforce, seamlessly integrated into our client's teams to execute the trial management of their trial portfolio.
Within a trial management FSP program, innovations in technology and analytics enable key tasks and activities to be completed centrally, such as removing administrative burden to low cost centralized locations and rethinking traditional trial management tasks, offering incremental improvements to derive more value.
Trial Management
Trial Management
Driving value by innovating the way you manage trials
IQVIA's FSP programs successfully deliver various functional trial management solutions, identifying and staffing key leadership roles with global project management experience. We provide a flexible and dedicated workforce, seamlessly integrated into our client's teams to execute the trial management of their trial portfolio.
Within a trial management FSP program, innovations in technology and analytics enable key tasks and activities to be completed centrally, such as removing administrative burden to low cost centralized locations and rethinking traditional trial management tasks, offering incremental improvements to derive more value.
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