Statistical Support

ACRO understands that having the right statistician on your team is critical to your study design, conduct, and overall analysis. Ensuring appropriate design and analysis maximizes your data quality and reliability, and overall, minimizes the risk of data rejection by your regulatory agency or agencies. ACRO provides the following statistical support:

Trial design consultation
Protocol review and feedback
Development and maintenance of study-specific Statistical Analysis Plans
Development and management of randomization plans when applicable
Data standardization to conform to CDISC standards
CDISC data validation to ensure FDA data submission requirements are met
Data analysis following acceptable industry data analysis standards
Participate in project/regulatory agency meetings as needed