Data Management + Biostats

|Data Management + Biostats
Data Management + Biostats 2018-01-18T21:01:54+00:00
What We Do

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.

Medical device/imaging studies
Oncological indications
Orphan drug approvals

Count on our clinical expertise, cross-functionality, and flexible workflows to help you:

  • Expedite trial start with our four-week database build timeline – 2x faster than the industry standard
  • Increase efficiency with robust cross-functional training of all team members
  • Provide data management and biostatistics experts who have also undertaken extensive physician-led protocol training for each project (at no sponsor charge)
  • Deliver high-quality results with QC and double programming implemented into all QA processes
  • Ensure accurate medical coding from a fully-trained medical coding team
“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 Management & Biostatistics 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?