At Cesta Inc., our biostatisticians and programmers bring a wealth of experience to the clinical research industry. Each team member holds a graduate degree and possesses over ten years of hands-on experience within the pharmaceutical and Contract Research Organization (CRO) sector. This collective expertise empowers us to offer a comprehensive array of services to clients engaged in all phases of clinical trials. We firmly believe that integrating our biostatisticians and programmers at any stage of a clinical trial significantly enhances the likelihood of its successful and timely completion with a high standard of quality.

Key aspects of our Biostatistics and SAS® offerings include:

Study design, sample size calculation, and protocol development.

Assistance in creating Case Report Forms (CRFs).

Development of bio-statistical analysis plans.

Biostatistical analysis and SAS programming/analytical proficiency.

Generation of analysis datasets.

Implementation of CDISC Standards for SDTM and ADAM Datasets.

Validation of data sets to ensure accuracy and completeness.

Creation of integrated clinical reports covering safety, efficacy, and new drug application.

Electronic submission of protocol and study results to the FDA.

Assistance in writing final clinical study reports.

Our commitment revolves around delivering accurate reports punctually, executed with professionalism and integrity. Understanding and addressing the unique needs of our clients remain at the core of our goals.

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

Contact Us