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ClinAccess™ Overview
ClinAccess™ 5.1 is the next generation of the industry leading Clinical Data Management System based entirely on SAS® 9. It leads the way in simplifying clinical data management, clinical trial analysis and preparation of electronic submissions. Having your data keyed directly into SAS® data sets enhances your staff’s productivity. ClinAccess™ is designed expressly for ease-of-use data entry and management with features to monitor the progress and quality of ongoing clinical trials. Whether for review, analysis, or FDA submission, your data is always in SAS®. The database structure is designed to support and accelerate statistical analysis and reporting. The result is less time and effort for data analysis and a shorter time to market. For reliability, auditing and security, there is no better solution than ClinAccess™.
Additionally, our system provides greater flexibility in handling unique situations with a highly affordable return on investment. The result is ClinAccess™ allows you to achieve your clinical trial goals faster, with greater ease at lower cost.
Features of the ClinAccess™5.1 integrated solution include:
- Study Definition
- 16 Types of Data Entry (including Double-Key Entry and
a complete Audit Trail).
- CRF Imaging
- Forms Control
- Query Capture, Reporting, and Resolution
- Dictionary Coding of Adverse Events (AEs) & Medical Terms
- Clinical Data Review Tools
- 21 CFR Part 11 and CDISC Compliant
- Prepares Data and CRF Images to FDA e-Submission Standards
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