Product/Service

Biometrics

Source: Theorem Clinical Research
Our Biometrics professionals are statisticians and programmers who do more than just crunch numbers. They operate as your partner from the very beginning, working with you to determine the endpoints to analyze, statistical procedures, evaluation criteria, patient subsets, and data display formats.

Our Biometrics professionals are statisticians and programmers who do more than just crunch numbers. They operate as your partner from the very beginning, working with you to determine the endpoints to analyze, statistical procedures, evaluation criteria, patient subsets, and data display formats. Not to mention, we're closely involved throughout the entire process with our colleagues in Project Management, Clinical Writing and Clinical Data Management—and, most importantly, you.

  • Customized Services. We provide the services you need to ensure high-quality, rapid turnaround of interim and final trial results—in both electronic and paper versions:
    • Protocol and Analysis Plan Development
    • Data Analysis and Reporting
    • CDISC Standardization and Submissions—in fact, CDISC recently designated our Biometrics team a Registered Solutions Provider!
    • Clinical Study reports
    • Data Monitoring and Committee Support
  • Statistical Experts. Our Biometrics professionals have an average of nine years' experience and a comprehensive scope of therapeutic expertise. It's that level of knowledge that enables our statisticians and programmers to quickly deliver high-quality work. For example, you can expect key results within 48 hours of hard database lock—and full results within one week.
  • Real-Time Analyses. Using our secure clinical trial portal, OmniView, you'll have ready access to your tables and listings on demand—without compromising the blinded nature of the study. Our people utilize a variety of leading industry software packages to interpret results.
  • Superior Quality. The integrity of your data lies in our hands and you can trust our focus on quality. As part of our process, we hold a Round Table Meeting with you to review all tables and listings at 50 percent of data collection. This milestone enables you to make any adjustments due to unexpected study circumstances—and it allows us to provide feedback to Clinical Monitoring, Data Management, and Clinical Writing. Also, we feature online quality control documentation and dynamic audit trails.
  • Global Approach. Our ever-growing data centers are strategically located around the globe in Australia, Germany, India, the United Kingdom and the United States. Centralized systems and communication maintain a constant flow of information.