Corrective And Preventative Action
Save Time, Resources and Money by Implementing Ready-CAPA™
Ready-CAPA™ allows you to track issues, observations, incidents and improvements in a structured manner, meeting regulatory requirements for CAPA.
At a fraction of the cost charged by competing systems, Ready-CAPA can be rapidly deployed as a pre-configured validated package.
Ready-CAPA is a reasonably priced solution that provides you with:
- CAPA Lifecycle Management
- Action Planning
- Past Due Alerts
- Root Cause Tracking
- Performance Reporting
- Trending
- Audit Trail Management
- Role Based Security
- Validation Package
- 21CFR Part 11 Compliance
- Hosted or On-premise Options
|
Demonstration Video
|
Screenshot Gallery
|
|
|
|
Fully Automated CAPA Management System
Most regulatory agencies view the CAPA process as the central component to resolve incidents that affect product safety, quality, integrity, potency or purity. Over 50% of the top 10 FDA cGMP inspectional observations were related to insufficient CAPA processes.
Organizations cannot afford to continue tracking issues and investigations via spreadsheets or simple databases. Regulatory agencies are enforcing the resolution of compliance and CAPA related issues more than ever. Are You Ready?
|
