Biostatistics
Our Biostatistician services are designed to be your dedicated partner for achieving precision in every aspect of clinical research projects.
With a focus on innovative study designs, effective randomization
processes, and thorough data analyses, we ensure the reliability of your results and provide clear
interpretation through comprehensive statistical analysis plans. Our commitment extends to generating
detailed statistical reports, contributing to Clinical Study Reports, and leveraging cutting-edge
technology for accurate and timely data analysis.
Our Specialized
Biostatistical Expertise Covers:
In the context of our services, we specialize in oncology and various therapeutic areas. Regulatory
compliance, seamless collaboration with research teams, and a continuous improvement approach
define our services. From adaptive trial designs to Bayesian methodologies and rigorous quality control,
our Biostatistician services deliver valuable insights and recommendations throughout the research
process, elevating the success of your clinical trials.
Protocol development
Study design
Power calculations
Analysis and endpoint strategies
PK/PD analyses and modeling
Observational Studies/RWE
Writing statistical sections of the protocol and clinical study report
Tables, listings, and figures
Support for data safety monitoring board and independent data monitoring committees
Non-compartmental pharmacokinetic and pharmacodynamics analysis
Integrated summaries of efficacy and safety/CSR
Annual reports/DSURs
Our Specialized
Biostatistical Expertise Covers:
In the context of our services, we specialize in oncology and various therapeutic areas. Regulatory
compliance, seamless collaboration with research teams, and a continuous improvement approach
define our services. From adaptive trial designs to Bayesian methodologies and rigorous quality control,
our Biostatistician services deliver valuable insights and recommendations throughout the research
process, elevating the success of your clinical trials.
Protocol development
Study design
Power calculations
Analysis and endpoint strategies
PK/PD analyses and modeling
Observational Studies/RWE
Writing statistical sections of the protocol and clinical study report
Tables, listings, and figures
Support for data safety monitoring board and independent data monitoring committees
Non-compartmental pharmacokinetic and pharmacodynamics analysis
Integrated summaries of efficacy and safety/CSR
