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 ClinAccess5.1 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