Cesta Inc. biostatisticians and programmers have extensive experience in the clinical research industry. All of our team members have at least a graduate degree and ten plus years of experience working in the pharmaceutical and CRO industry. The combined breadth of knowledge allows us to provide a full range of services to our clients involved in conducting all phases of clinical trials. We believe the inclusion of our biostatisticians and programmers in any stage of a clinical trial ensures its success of being completed efficiently and on time with high quality.

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Our Biostatistics and SAS® offerings are:

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• Study design, sample size calculation, and Protocol development

• Assisting with creation of Case Report Forms (CRFs)

• Creation of bio-statistical analysis plans

• Biostatistical analysis and SAS programming/analytical expertise

• Creation of analysis datasets

• Implementation of CDISC Standards for the creation of SDTM and ADAM Datasets

• Validation of data sets to ensure accuracy and completeness

• Creation of integrated clinical reports (safety, efficacy and new drug application)

• Provide electronic submission of protocol and study results to FDA

• Assist in writing of final clinical study reports​

Delivering accurate reports on time, with professionalism and integrity, is our focus. Understanding and addressing our client’s needs are our goals.

Contact one of our Consulting professionals today to see how we can help you.