We deliver what you need
Biostatistics is a key element of a clinical trial and needs to be handled with expertise and attention to details.
InnoPharma understands your specific requirements and provides an exceptional level of service, whether the request is an integral part of a full clinical trial program, or as a stand-alone consulting or training service, InnoPharma biostatisticians and consultants can quickly step in to make significant contributions to your study, ensuring that your project gets the individual attention it deserves.
All design, analysis and reporting is based on ICH guidelines, client needs, and our own procedures. Rigorous QC methods are employed at all stages.
- Statistical aspects of study design
Input into protocol
Sample size calculations
CRF design review
- Statistical analysis planning
Analysis planning meetings
Methodology development and evaluation
Production of analysis plan
- Data analysis
Analysis, table, figure and appendix programming
Blind review of protocol violations
Independing QC through double programming and peer review
Integrated clinical and statistical reports