Our clinical data management experts provide unrivaled speed, flexibility, and quality
Clinical Trial Data Management has been a cornerstone of our clinical research services for more than 30 years. We have spent the last 3 decades sharpening our skills and processes to consistently deliver databases of the highest quality with unmatched speed and flexibility. The Rho clinical data management staff is well versed in good clinical data management practices (GCDMP) and has strong technical, programming, and communication skills. Whether your clinical trial is a multi-site post-marketing study with thousands of subjects or a single center Phase I study with fewer than 50 subjects, Rho's clinical data management team will provide a customized, cost-effective, and flexible approach to meet all of your data management needs.
Data collection that meets our clients' needs
Paper or electronic data capture (EDC)? Should Clinical data acquisition standards harmonization (CDASH) standards be used? Rho understands that navigating today's data collection and submission landscape can be complicated. Well-informed decisions about your study's data can save time and money later in your program. Rho's clinical data management experts can advise you on the best path for your study and can implement data collection and formatting strategies to maximize your investment.
Electronic data capture: Rho can recommend an EDC strategy that's right for your program. Our staff has extensive experience providing data management services using multiple EDC systems and can collaborate with you to choose the option that best meets your program's needs. Whatever the technology, Rho staff will ensure the database and validation checks are deployed quickly, that sites and users are trained on the system, and that results are available in a clean database, which is locked on time.
Paper-based data capture: If paper is the best choice for your program, Rho offers robust data collection using paper case report forms (CRFs). Rho's proprietary clinical data management system, RhoDMS™, ensures fast and flexible setup and consistently clean data. 21 CFR Part 11 compliant, our clinical data management system provides for CRF inventory and tracking at the page level, true independent double data entry with a third-party referee, and strong custom reporting. Queries are generated at the variable level to ensure pinpoint accuracy, and our databases consistently have less than 1 error in 10,000 analyzable fields.
Data formats and FDA submissions: Need advice on the best format for your data? Our Data Managers are experts in data standards. We can evaluate your entire program to help you determine the best format for your project's data and expedite the eventual creation and approval of your submission package. We can also convert legacy data to the most current standards.
Specialized expertise in medical coding and clinical trial data management programming
At Rho, medical coding is performed by a team of physicians and registered nurses. Specific coding rules can be applied at the sponsor, project, or individual event level to ensure consistency and accuracy across your entire program. In addition, our medical coders are expert clinical resources for our clinical data management staff.
Our comprehensive clinical data management services include:
- Clinical data management consulting
- CRF/eCRF design
- Database development & deployment
- Data entry and tracking
- Customized clinical data management programming
- Third-party data integration
- Knowledge and use of current data standards (SDTM, CDASH, and other CDISC standards)
- Data conversion to proprietary data specifications
- Interim analysis readiness
- Medical coding and serious adverse event (SAE) reconciliation
- Customized status reporting and data listings
- Database closeout and delivery
- Clinical trial rescue services
- Government/Non-governmental organization (NGO) projects