Clinical Trial Management
The Clinicals solution captures and reviews all trial-related information throughout the setup, conduct, and review of clinical trials. It is a highly scalable platform that is being used by some of the world's largest pharmaceutical companies and clinical research organizations (CROs) to manage their multiple global clinical trials, as well as by smaller biotechnology companies and academic research centers.
- Organize all trial-related documents, forms, and other records in a single global repository
- Provide qualified personnel with immediate access to every document, including CRFs, regardless of whether originally in paper or electronic form
- Leverage a fully auditable review process
- Achieve easier validation and maintenance of compliance
Key Performance Indicators
- Consistent processes between trials and with partners
- Global availability of information and trial status
- Full auditing for compliance
OpenText Clinical Trial Management delivers this functionality with the following components:
- Software: Clinicals, Document Management, Project Management, Records Management
Supplemented by Business Content (e.g., predefined workflows) to give you a head-start in configuring workstreams and processes, Consulting Services, Training and Support tailored to meet your requirements.
