Statistics & Programming
Boost your statistics with us
Excel in your statistics from protocol to publication: Cytech’s expert statisticians and programmers are here to ensure your reporting and analysis drive your study forward.
Our Services
Statistics and programming: trusted analytics at your fingertips
Statistics and biostatistics are central to your clinical trial, from planning and protocol through the study to publication and post-marketing pharmacovigilance.
Regulatory authorities need certain statistical information to approve your trial application, you generate biostatistics throughout the trial, and you need accurate, unbiased analyses to understand the results and get your intervention to those who need it.
With the support of our statistics experts, you can make sure you have the information you need at every stage of your trial.
At Cytech, we understand your information needs, and our experts are committed to ensuring your statistical analysis delivers error-free and unbiased results.
We prioritize the integrity of your research.
Accuracy and Reliability in Data
Numbers are the backbone of your research, and partnering with Cytech means we share the responsibility of ensuring your data is both accurate and impartial. We guarantee you have the statistical information you and your stakeholders require at every phase, from regulatory submissions to publication.
No matter the task, we operate transparently, meticulously accounting for every data point. Our harmonized processes and unified platforms ensure that your clinical analysis remains consistent and dependable. Plus, we leverage advanced technology to ensure the programming serves your needs effectively.
Comprehensive Statistical Analysis Solutions
Our biostatisticians offer a flexible, tailored approach to support your project. The Cytech team seamlessly integrates with yours, assisting with statistical tasks throughout your clinical trial’s lifecycle.
Design Phase
We help you plan your study from a statistical standpoint, including identifying necessary data capture, treatment arms, and potential adaptive designs. Our experts calculate sample sizes, conduct power analyses, and create statistical analysis plans to establish a solid foundation and optimize trial design.
Conduct Phase
Our biostatisticians work to eliminate bias in your study and conduct interim analyses. Collaborating closely with our Data Management teams ensures data integrity. We assist in determining blinding strategies and work with independent data review and safety committees (iDMC, DSMB, SRC) to monitor study safety.
Closing Phase
Cytech’s experts guide your team through the closing phase, interpreting results and deliverables to ensure that your medical conclusions are aligned with your study data.
Our comprehensive data management support is available at three levels: Resourcing, FSP (Functional Service Provider), and Full Service, tailored to meet your specific needs.