BIO-STATISTICS AND SAS

Only the Best

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.

Our Biostatistics and SAS® offerings are:

  • 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.