Validation to match every pharmaceutical business.
Life Science manufacturers walk a fine line as they try to balance the implementation of quality and regulatory compliance processes without breaking the bank. Using CDC Software's Ross ERP to automate document control systems, corrective action and preventive action (CAPA) processes, training control, and other quality management initiatives, manufacturers are achieving the results they need.
With Ross ERP, you have integrated quality and compliance management software systems for FDA and ISO regulated industries.
Solution Brochure: Ross Enterprise for the Life Science Industry
Key Features:
- Audits
- Change Control
- Customer Complaint Handling
- Corrective Action Preventive Action (CAPA)
- Document Control
- Engineering Change Control
- FDA eSubmissions
- Forms
- Portal
- Training Management/Tracking
- Validation
Here’s what Ross ERP for Life Sciences solutions can do for you:
Powerful Capabilities
Easy-to-use, integrated quality and compliance management solutions that help companies automate FDA and ISO-based quality processes.
Flexible Solutions
Because CDC is more than just a software company, we also offer implementation, training, and validation services to maximize our customers' efficiencies and savings.
