Clinical Trials are complex and time consuming. There are too many activities to be performed. The activities are diverse in nature and are interdependent. Clinical Trials are a single most expensive component of the entire drug development process. The Clinical Trials Management System (CTMS), designed and developed by CBS, is a centralized system that caters to operational and administrative activities of Clinical trials.

These are resource-intensive areas and often involve tedious, manual processes for collecting, aggregating and rationalizing information from a wide variety of data sources. It is difficult for CROs, Pharmaceutical companies and biopharmaceutical companies to organize and manage the heavy manpower requirement, medical appliances and other resources. The CTMS with its set of modules caters to this complex need intelligently. Information islands generated by different appliances need to be collated.

CTMS makes it possible through data migration modules. This allows the sponsoring organizations to streamline processes appropriately while comparing different platforms and proactively manage their trials. This way CTMS helps to improve operational efficiency and bring down overall time and cost requirements.

Key features:

  • Improves staff productivity and accuracy in study proposals, initiation, monitoring, and conclusion
  • Enhances efficiency of study site recruitment and study protocol compliance
  • Enables real time financial oversight, the fully web based and comprehensive simple and Intuitive User Interface
  • Improves staff productivity and accuracy in study proposals, initiation, monitoring, and conclusion
  • Enhances efficiency of study site recruitment and study protocol compliance
  • Enables real time financial oversight through centralized budget and expenditure tracking
  • Provide role-based access to users through centralized budget and expenditure tracking