OPTIMIZE TESTING TIME AND COSTS
We aid you with operational and strategic statistics needed for every aspect of drug development.
Are your legacy systems holding you back? We manage your design to implementation, integration, deployment, and management.
- Power analysis, definition of populations.
- Analysis plans.
- Contribute to CSR, ISS/ISE, DSUR, etc.
- CDISC format deliverables
Efficient Bio Statistical Reports
- Through Data Study
- Interim Planning
- Data Management
- Reporting Clinical data
Utilize our Statistical Programming expertise to enhance your clinical trials on every stage. We are through at analyzing clinical trial data to deliver concise and compliant outputs. A Project Manager will coordinate from inception to delivery, resource allocation, to timelines, budgets, and quality. Our Lead Programmers contribute in managing specific tasks on a subset of the project.
Our SAS programmers are always in demand as we ensure quality delivery, on time. QC Verification/Validation, SAS programming, Standard Operating Procedures (SOPs), and IT Projects are examples of the work typically performed by our experts.