The CRS Trial Management Lifecycle CRS Clinical Rater Station Lifecycle Diagram CRS Clinical Rater Station CRS Clinical Rater Station CRS Clinical Research Expertise CRS Clinical Research Expertise CRS Clinical Resesarch Expertise CRS Clinical Research Expertise Rater Training & Certificiation Rater Training & Certification Subject Qualification Rater Monitoring & Management Data Analysis & Reporting Subject Qualification Data Analysis & Reporting Rater Training & Certification Rater Training & Certification Rater Training & Certification Rater Monitoring & Management Rater Monitoring & Management

Products & Services

Concordant Rater Systems (CRS) offers a patented methodology and product* suite to improve the quality, efficiency and integrity of CNS clinical research. To achieve reliable results, the CRS approach follows our defined methodology of the four phase CRS Trial Management Lifecycle, with supporting products and services.

Our solutions lead the industry in the management of clinical trials by addressing some inherent problems of the drug development process which relies on clinical assessment using subjective scales and the resulting inconsistency that can be difficult to recognize and rectify in a timely manner. We address widespread issues such as rater reliability, high placebo response rates, subject enrollment pressures and assessment variability, that contribute to failed studies.

CRS Solutions Summary

Client Issues/Needs CRS Solution
  • Assessment Selection
  • Site Selection (US or ROW)
  • Study Design
 Clinical Research Expertise
  • Standardize rater performance on assessments
 Rater Training & Certification
  • Enhance diagnostic precision and confidence for subject inclusion
 Subject Qualification
  • In-study rater reliability and quality assurance
  • Early identification of underperforming sites and raters
 Rater Monitoring & Management
  • High placebo response
  • Baseline inflation
  • Cost-effective and efficient study management
  • Scalable solution in multiple languages
  • Real-time access to data and reports
 CRS Trial Management Lifecycle Solution

CRS views data, timely access to data, and consistency as key drivers in the achievement of trusted outcomes. Our methodology and product suite is designed to ensure consistency throughout a trial and to enable real-time access to data so clients can make informed decisions and take corrective action immediately.

Our core product, the CRS Clinical Rater Station, is our platform that delivers our products, and supports the methodology and services of the CRS Trial Management Lifecycle. CRS Trial Management Lifecycle products and services include:

*CRS patent 7,315,725 B2; “Computer system and method for training, certifying and monitoring human clinical raters.”