| Services Overview |
XTrials Research professionals consistently apply their process planning, regulatory, and clinical operations expertise to
deliver high quality clinical work products by streamlining the clinical trial process and facilitating effective communication
among functional resources.
All clinical projects present unique challenges while navigating the complexities of global regulatory requirements and demands
for optimal performance. Our project teams are well-trained and experienced in anticipating potential challenges and mitigating
risks by acting proactively to apply intelligent solutions to effectively manage timely outcomes. From study start-up to
completion, our knowledgeable research professionals bring the flexibility, insight, and creative problem-solving needed to
confidently achieve our Clients' objectives, prevent delays, and exceed expectations.
Our proprietary InFuse™ eClinical environment provides the operational backbone for delivering this agile performance. It
provides direct access to process tracking, maximizes visibility to clinical data, and facilitates efficient collaboration
among study team members. It is this effective mix of expert talent, efficient process and innovative technology that translates
into cost-effective pricing and enables us to consistently bring your projects in
on-time, on-target, and on-budget.
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| Project Management |
We provide full project management support for Phase I through Phase IV Drug and all phases of Medical Device trials across
the major therapeutic indications.
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| Study Start-up |
We have proven procedures and electronic support facilities to expedite the selection and qualification of clinical sites that
exhibit high probabilities of "showing up to play".
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| Clinical Monitoring |
We offer comprehensive site monitoring support from site initiation to completion. Our CRAs are fully trained in
FDA regulations, ICH guidelines, GCP compliance, data review, and site management.
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| Medical Monitoring |
Our medical monitors serve all phases of clinical development and work closely with Sponsor Management and internal
project teams throughout the course of the clinical program.
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| Clinical Development |
These days everybody is doing more with less. From First-in-Human to pivotal Phase III trials, our expert
professionals are dedicated to bringing the best value for your clinical development budgets.
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| Medical Devices |
Thousands of medical devices and in-vitro diagnostics are being developed and commercialized.
Many providers do not recognize key differences from supporting pharmaceutical requirements. We do.
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| Late Phase |
From prospective post-market studies to disease and product registries or retrospective analysis studies,
we bring the experience, technology, and insights needed to make your marketing programs a success.
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| Functional Services |
The FSP model is gaining increased traction as Sponsors endeavor to achieve significant improvements in cost
efficiencies. We have been providing expert functional services support for over two decades.
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