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Biometrics Expertise for Clinical Trials and Regulatory Submissions

Advancing a novel therapy through clinical development is complicated.   Not all therapies make it to the patients that need them, not because they did not work, but because the design, data collection and/or analysis were not done right. Correctly designing, collecting, analyzing, standardizing, and reporting your clinical trial data to local and global regulatory agencies is critical to your success. To give you an advantage, Veristat has assembled an extraordinary team of scientific-minded biostatisticians, programmers, data managers and data standards experts, the power of industry-leading technology platforms and expertise in adaptive designs, to help you understand your data to make critical clinical development decisions.

clinical trial data collection and data managment

Data Management

Find out how we design, build, and deploy clinical databases faster than the industry norm.

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biostatistics for clinical trials - regulatory submissions

Biostatistics

Discover how our biostatisticians work closely with the entire project team throughout your study to ensure that the correct data is captured and ready for analysis.

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statistical programming of clinical trial analysis datasets and TLFs

Statistical Programming

Learn how our programmers perform your planned analyses including the creation and QC of analysis datasets and tables, listings, and figures.

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clinical trial CDISC data standardization

Data Standards Implementation

Understand how we can help your company make CDISC compliant data standards implementation and migration seamless.

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