Clinical Trial

FORM MODULE
Enables the user to enter dual key CRFs.
Ability for comparison of data between two keys to insure accurate data input.
Printer friendly mode.
All entries are user and date stamped, making audits easy.
All errors and modifications are logged in database.
Ranges can be inputted to generate reports on the fly of abnormal data.

SECURITY MODULE
Allows the configuration of unlimited employees and access groups.
Security design complies with 21 CFR 11 FDA Guidance on Computerized Systems Used iin Clinical Trials.
Changes in security level. users and login attepmts are logged to the database for audits.

SITE AND PATIENT MODULE
Allows easy inputting of testing sites and patients.
Patients data conform to HIPAA standards
Keeps track of demographic data as well as Surgery Dates, Implanted Eye, etc…
For sites, keeps track of demographic data plus miscellaneous info such as IRB Approvals and Renewals

REPORT MODULE
Core of application. Data is meaningless unless it can be interpreted in a report fashion.
Report Builder allows the user to access any and all data in an Excel Spreadsheet Format.
Printer friendly mode.
Built in reports have Summary and Detail Mode.
Custom Reports can be built with Crystal Reports

ADMINISTRATOR MODULE
Create CRFs for the system on the fly!  Includes the ability to create data fields and layout CRF screens.
Field selector for built in reports
Group Manager - Allows the administrator to create custom security groups
Access Export - All or selected data can be exported to an Access Database