Global
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日本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
Open Text 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, コンサルティングサービス, トレーニング and サポート tailored to meet your requirements.
Key Performance Indicators
Consistent processes between trials and with partners
Global availability of information and trial status
Full auditing for compliance
