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Services

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, standardizing, analyzing, 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.

Veristat. The Science-First CRO.

Submit Your RFP     Contact Our Experts

Integrated Biometrics Solutions Across the Development and Commercialization Lifecycle

Clinical Trial Data Management Services
Data Management

Accelerating the design, build, and deployment of clinical trial databases faster than the industry norm. 

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Biostatistical Consulting for Clinical Trials
Biostatistics

Expert statistical planning and analysis to ensure clinical development success. 

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statistical programming for clinical trials
Statistical Programming

Speed, quality, and expert programming to perform accurate clinical trial data sets for analysis.

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clinical trial data standardization into SDTM and ADaM format
Data Standardization

Preparing clinical trial data into submission-ready format for regulatory agencies/authorities around the world.

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Data Safety Review Committe
Data Monitoring Committees

Improve patient safety and reduce risks with proven and acceptable independent DMC models and administration best practices.

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biostatistics resourcing, functional service provider, FSP
FSP/Resourcing

Finding the right resources to meet your development program’s milestones and accelerate time to market is critical today.

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