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Fast, flexible, and exceptional quality. Meet the fully integrated clinical data management team that actually delivers. Real-time data status and extraction with standard and customized reports.
Expedite trial start with our agile approach to database build that is platform agnostic. We consistently achieve a build-and-release timeline that exceeds the industry standard. And our highly experienced and integrated team remains responsive to protocol changes, ensuring continual quality as well as CDISC and 21 CFR Part 11 compliance.
Achieve faster EDC builds and enjoy the electronic data capture platform of your choice. Our clinical data team members have deep technical expertise across multiple EDCs.
Our PhD- and MS-level professionals, including pharma veterans, all have comprehensive therapeutic experience and interdisciplinary skills they bring to each and every study.
Firma is the first choice for study rescue for a reason. Every engagement is driven by a commitment to not just meeting deadlines but beating them. At Firma, turn-around-times are sacrosanct.
A stable team creates continuity and consistency which are the foundation of a high-quality and efficient clinical data management.
From study startup to submission, your Firma team collaborates closely with the clinical team. Our cross-functional team environment, real study training, continuous education, high quality SAS programs, unique programming and more all contribute to our ability to meet or exceed timelines.
Find out how Firma uses a lifecycle approach and why it is key to delivering a compelling data story to FDA, so it is easily understood for rapid approval and accurate labeling.
