Medfiles Global is your direct source for comprehensive biostatistics and statistical programming.
Our statisticians have decades of industry experience providing prompt and accurate reports, statistical summaries, and efficacy and safety analyses. From the initial stage of study design and planning to final stages of data analysis and interpretation, it’s easy with Medfiles Global.
Our statistical expertise includes:
- Statistical consulting for product development and regulatory defense
- Clinical trial randomization services
- Sample size and power calculations
- Statistical analysis report writing for clinical study reports and/or manuscripts
- Integrated efficacy and safety summaries
- Multifaceted statistical approaches including pooled analyses and meta-analyses
- Detailed statistical input for protocols and evaluations
- Detailed statistical analysis plans (SAPs) and table designs
Medfiles Global knows SAS®, having built entire applications for the clinical trial industry using the software. Our team provides scalable statistical support, and we have highly qualified, seasoned programmers who ensure flexibility to meet your unique needs and internal guidelines. We can work with your templates or our‘s, or we can create a set of programming templates specific to your organization.
For more information please contact
Clinical Research Services
+358 20 744 1504 / firstname.lastname@example.org