FMD K&L biostatisticians provide a keen understanding of every aspect of clinical development programs
With an efficient organizational structure designed to promote high-quality standards, we deploy a group of broadly experienced biostatisticians with in‐depth expertise in various therapeutic areas. We assist pharmaceutical, biotechnology, and medical device sponsor companies to navigate complex and dynamic processes en route to product approval.
- Clinical development planning
- Power/sample size estimation
- Protocol development
- Statistical analysis planning
- Randomization scheduling
- Interim analysis/DMC
- Annual or periodic reporting
- Statistical modeling/exploratory analysis
- Statistical reporting and publications
- Clinical study reporting
Our team is dedicated to supporting your achievement of full insight from your clinical trial data. We approach every project with a commitment to work tirelessly to ensure accurate data, careful analysis, and concise presentations, all within timelines and budgets.
These services are available individually or as part of an end-to-end solution.