Speed regulatory submissions with efficient, high-quality data and analyses
Ensure accurate study results and speed quality submissions by leveraging our vast clinical experience. Our team consists of PhD- and MS-level professionals adhering to a single set of global standard operating procedures, offering their detailed and extensive knowledge of pharmaceutical development to benefit your entire data management and biostatistics planning, execution, and analysis. Our approach to data management and biostatistics begins with a broad knowledge base in all aspects of the clinical trial process and a dedication to cross-training all team members prior to initiation of the study.
Data Management and Biostatistics experience you can count on.
“Firma delivers when they commit to a study. The quality of their work is always high and they have never missed a timeline regardless of protocol amendments throughout the study lifecycle.”