Technology solutions that provide efficiency to clinical trial management
Rho utilizes a combination of proprietary applications and partnerships with third-party providers to offer our clients technology solutions that meet our high standards of quality. Our integrated technology solutions increase our flexibility and maximize efficiency for your clinical trial project or program.
Proprietary technology solutions built on years of clinical research experience
The success of our proprietary technology solutions is a result of our industry-defining work in statistics, clinical data management, and project management in more than 25 years of support of clinical research. Our technology solutions were built from an early and consistent commitment to apply our knowledge and experience to tools that improve the way we deliver services. Our proprietary solutions comply with applicable regulations and industry standards, including 21 CFR Part 11.
Technology solutions that make the most sense for our clients
When working with our clients to choose or recommend a tool, our first responsibility is to provide our clients with the right solution, regardless of brand. Whether it's one of ours or a third-party tool, we consider speed, flexibility, pricing, and ability to integrate with existing tools.
Below are some of the most popular technology solutions Rho offers:
Deploy a more powerful, accessible, and reliable randomization system
Our Web and voice randomization, patient diary, and notification systems use state-of-the-art technology to manage clinical trials. RhoRAND™ is sponsor customized to meet the specific needs of any trial. It provides simple data collection for subject enrollment and randomization using a touch-tone phone or Web browser. RhoRAND™ ensures protection of vital study data with user authentication protocols, dedicated servers, and remote network backup. It also comes with 24-hour, multilingual support.
A robust EDC/CDM solution to manage your clinical trial data Medidata Rave® is an advanced and robust system for capturing, managing and reporting clinical research data, designed to help life science companies optimize their research investments by efficiently streamlining the clinical trial process. Rave's single EDC/CDM platform, coupled with high scalability and software-as-a-service (SaaS) architecture, provides a cost-effective approach to quickly implement a single clinical trial or support an enterprise-wide deployment for multiple therapeutic areas, phases and studies. The wide-support of industry standards and a rich set of on-demand data extraction and reporting tools provide a robust platform to manage site-, patient- and lab reported data and rapidly make it available for analysis and submission.
A comprehensive solution for pharmacovigilance Oracle® Argus Safety is an advanced and comprehensive pharmacovigilance software system. An off-the-shelf, web-based software package, Argus provides the collection, tracking, reporting, and analyzing of adverse events and serious adverse events for drugs, biologics/vaccines, and devices in accordance with global regulatory requirements. It ensures the integrity and confidentiality of safety data used in support of regulatory submissions.
Argus provides a robust library of reports and the flexibility to create ad-hoc reports to meet sponsor and project needs for safety data analysis. The ease of database configuration allows for quick start-up and ongoing addition of studies, products, and sites. Argus Safety and Rho Product Safety provide a centralized, global safety solution for the life cycle of a product from early clinical development through post marketing.