Trial Design Solutions
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Experience The Benefits Of Conducting Your Next Study In Eastern Europe
8/13/2021
OCT Clinical, one of the leading CROs in Eastern Europe, offers a full range of services for Phase I-IV and BE studies, including study design, regulatory support, site management and more. We know how to conduct your trial seamlessly: on budget and on time.
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IQVIA Biotech Virtual Clinical Trials
3/4/2021
IQVIA Biotech virtual trials speed recruitment, heighten retention, and improve data quality by leveraging our transformative technology, unparalleled data, and therapeutic expertise. With experience designing and delivering complex hybrid studies and 100% virtual trials across the United States, Europe and Asia, IQVIA Biotech helps emerging biopharma and biotech customers accelerate timelines and achieve study goals.
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Your Oncology CRO Dilemma Solved
7/27/2022
Uncover the details of this go-to solution from a leading Eastern European CRO that is capable of ensuring timely enrollment and study success.
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Driving Successful In CNS And Neurology Trials
9/20/2023
Second, only to Oncology, CNS, and Neurology clinical trials are incredibly complex and complicated to navigate.
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Phlexglobal Experts Fill The Gaps In eTMF Management
12/16/2022
Enable busy study teams to assess, prevent, and manage risk across the entire TMF spectrum – improving inspection-readiness with less effort.
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Accelerate Clinical Trial Cycle Times With Citeline Study Feasibility
6/29/2021
Citeline Study Feasibility is a platform that combines subject-matter expertise and machine learning to develop predictive insights for feasibility planning. Clinical trial sponsors can use these insights to identify key data drivers and model their impact, build and simulate feasibility scenarios, accelerate timelines, and make better decisions than with statistical methods alone.
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Study Oversight & Analytics
2/21/2023
Discover how organizations can better visualize, analyze, and distribute aggregated and harmonized data to support study oversight, data analyses, and clinical reporting needs.
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Bold Thinking Overcomes Oncology Clinical Development Challenges
5/31/2022
Veristat ensures that your clinical trial or program design supports your regulatory strategy, whether you plan to run a single pivotal trial or multiple trials.
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Biorasi Rare and Urgent Disease
9/21/2021
Read how Biorasi's speed and agility make all the difference in overcoming unique obstacles to rare disease clinical trials.
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Signant SmartSignals® Advisory
5/15/2024
With the expert guidance of Signant's dedicated team of clinical science, medicine, and operations professionals, you can be assured that your protocol and endpoint data quality is safeguarded throughout your study's lifecycle.