Firma Clinical Research
Firma Clinical Research is a specialized contract research organization (CRO) dedicated to providing innovative clinical trial services, including decentralized and patient-centric approaches. They focus on supporting global, complex, and nontraditional study designs with a strong emphasis on data integrity, regulatory compliance, and patient diversity. Their mission is to facilitate efficient, flexible, and inclusive clinical research to bring therapies to patients faster and more effectively.
Industries
Nr. of Employees
medium (51-250)
Firma Clinical Research
Chicago, Illinois, United States, North America
Services
Networked delivery of protocol visits in patients' homes by trained clinical providers, covering sample collection, vitals, EKGs, questionnaires, study drug administration, and participant education, with PI oversight and logistical coordination.
Integrated data services including biostatistics, statistical programming, data management, EDC builds, QC processes, and deliverables for regulatory submission readiness.
Embedded, scalable teams of database builders, clinical data managers, medical coders, statistical programmers, and biostatisticians that operate as an extension of client teams.
Design and operationalization of decentralized trial elements including telehealth, eSource integration, remote sample collection, and hybrid/virtual visit models to reduce patient burden and broaden recruitment.
Database design and programming, CRF design, data cleaning, query management, medical coding, laboratory data integration, SDTM-compatible dataset export, and inspection support.
Rapid services to remediate at-risk studies, including fast database builds, programming of tables/figures, and creation of study report shells to meet regulatory timelines.
Networked delivery of protocol visits in patients' homes by trained clinical providers, covering sample collection, vitals, EKGs, questionnaires, study drug administration, and participant education, with PI oversight and logistical coordination.
Integrated data services including biostatistics, statistical programming, data management, EDC builds, QC processes, and deliverables for regulatory submission readiness.
Embedded, scalable teams of database builders, clinical data managers, medical coders, statistical programmers, and biostatisticians that operate as an extension of client teams.
Design and operationalization of decentralized trial elements including telehealth, eSource integration, remote sample collection, and hybrid/virtual visit models to reduce patient burden and broaden recruitment.
Database design and programming, CRF design, data cleaning, query management, medical coding, laboratory data integration, SDTM-compatible dataset export, and inspection support.
Rapid services to remediate at-risk studies, including fast database builds, programming of tables/figures, and creation of study report shells to meet regulatory timelines.
Expertise Areas
- Decentralized clinical trials (DCT) and in-home visit operations
- Clinical data management and EDC implementation
- Biostatistics and advanced statistical consulting
- Statistical programming and regulatory dataset preparation
Key Technologies
- Electronic data capture (EDC) systems
- eSource / direct data capture
- eCOA / electronic clinical outcome assessments
- Telehealth platforms for remote assessments
News & Updates
Answers to common questions about using remote, in-home visits in clinical trials, including IRB approval, liability insurance, oversight, and data handling.
Leadership discusses the advantages and challenges of using real-world data in clinical research.
Home Visits Completed
Over 30,000 home visits for decentralized clinical trial support.
Countries Covered
Support in more than 70 countries worldwide.
Answers to common questions about using remote, in-home visits in clinical trials, including IRB approval, liability insurance, oversight, and data handling.
Leadership discusses the advantages and challenges of using real-world data in clinical research.
Home Visits Completed
Over 30,000 home visits for decentralized clinical trial support.
Countries Covered
Support in more than 70 countries worldwide.