Working in an industry that relies on the collection of data using subjective scales leaves room for inconsistencies that are often too difficult to recognize and rectify in a timely manner. Widespread issues, such as rater reliability, high placebo response rates, subject enrollment pressures and assessment variability, can contribute to a failed study.
Avoid these pitfalls with strategic and technological support from Bracket. We’ve successfully managed more than 1,100 clinical trials, ranging in size from three sites to 1,500 sites, eight subjects to 26,000 subjects, and we can do the same for you. Let us help you address all aspects of your clinical rating instruments and data collecting needs with proven and patented methodologies that drive endpoint reliability. Improve the quality, efficiency and accuracy of your clinical research with constant monitoring, real-time feedback and guidance. With this level of transparency, you’ll be able to make timely decisions regarding your trial—decisions that will save you the time, cost and stress associated with the collection of inaccurate data.
Experience peace of mind knowing that you are getting the most out of our proprietary products, normative databases and best-in-class technologies.
Drive standardization and uniformity of diagnoses and clinical data with sophisticated in-study ratings reliability. Learn more >
Improve data quality and assure FDA compliance with continuous video and audio monitoring and support to sites and raters throughout your study. Learn more >
Increase precision and ratings reliability with computerized tandem-ratings, prompted assessments and diagnostic validation. Learn more >
Increase scoring standardization and precision with patient education materials.
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