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 data 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 study initiation.
Data Services 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.”
Learn how three clients relied on Firma Data Services to deliver speedy database integration and summary analyses to meet regulatory requirements.
Want to learn how you can speed regulatory submissions with efficient, high-quality data and analyses?