ACORN CRO is dedicated to providing access to the leading data management systems in the industry in order to meet the needs of our sponsors and sites more effectively and efficiently. Because of the system’s web-based design, it can provide real-time data access and monitoring resulting in cleaner data. User-friendly, intuitive navigation results in high user acceptance ratings. Other highlights include:
- Satisfies all applicable FDA Regulations, including 21 CFR, Part 11
- Supports all Phases of clinical trials
- 24/7 (EDC) Support Center
- Comprehensive end-user training via eLearning
- Electronic Case Report Form (eCRF) development using Clinical Data Acquisition Standards Harmonization (CDASH) standards
- Seamlessly supports mid-study changes
- Electronic signatures
- Capability to export data into multiple formats
- Point of entry data validations
- Increased feasibility of communication between sites, CRA and Data Manager
- Greater cost-effectiveness compared to paper and other EDC systems
- Ad-hoc reporting
- Access to Clinical Trial Management Systems (CTMS) and Safety modules
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