Quality Reimagined
Gain control and understanding of your global processes to drive compliance
QMS and Quality Documents Management on the CARA Life Sciences Platform™ brings all your quality divisions, content, data and processes together to create a modern quality landscape for your business.
A comprehensive guide to Quality on the CARA Life Sciences Platform
- Quality Documents Management
- QMS
- Quality Events
- Corrective and Preventive Actions (CAPAs)
- Change Controls
- Deviations
- Complaints
- Audit & Inspection Management
- LMS
Trying to drive compliance without standardised global processes and centralised information makes you the back-seat driver: unsure of the entire journey, and unable to control the direction of progress.
Instead, CARA for Quality creates a global community that shares processes and information, driving improvements across the organisation together.
“A superior customer experience, and a high level of quality and accuracy as the correct information is being captured at the source. It will also remove manual work for our internal people, resulting in a significant efficiency gain.”
Heiner Niessen,
Head of Global Quality and Quality IT Programs
Achieve excellence across your enterprise
Consistency
Take control of all your information with best practises across the board to reduce re-work and time wasted.
Connectivity
Leverage a centralised system for all your global processes with a cloud-first solution.
Proactivity
Automate work for your colleagues with collaboration and AI, ready for the challenges of tomorrow.
Visibility
Gain true oversight with easy reporting, dashboard and a ‘where-used’ system.
Consistency
Connectivity
Take control of all your information with best practises across the board to reduce re-work and time wasted.
Leverage a centralised system for all your global processes with a cloud-first solution.
Proactivity
Visibility
Automate work for your colleagues with collaboration and AI, ready for the challenges of tomorrow.
Gain true oversight with easy reporting, dashboard and a ‘where-used’ system.
All Together
If you’re just looking for a Quality DMS or stand-alone QMS, then you can just use those solutions – if you’re looking for a seamless Quality platform with Quality Content Management, QMS, LMS and Audit & Inspection Management, you’re also in the right place.
Quality Documents
Document creation, review, and approval with eSignature, periodic review, and effectiveness, and controlled printing. Video also supported.
QMS
Quality Events
Corrective and Preventive Actions (CAPAs)
Change Requests
Deviations
Complaints
Audit & Inspection Management
Automate, collaborate, and provide external partners with limited access to reduce manual work.
LMS
Seamlessly deliver approved content to your employees with LMS tied to QMS. Define courses, roles and curricula, as well as supporting external training
Latest Resources
Chemical Management on the CARA Life Sciences Platform
Chemical Management on the CARA Life Sciences Platform CARA streamlines the creation, storage, and lifecycle management of chemicals, raw materials, formulations, and packaging by integrating
The Next 5 Years with James Kelleher
Since founding Generis, James Kelleher has witnessed the company’s transformation from a boutique consultancy into a global leader in content and data management. We caught
CARA Platform Document Management Overview
The CARA Platform: Document Management Overview The CARA Platform streamlines document management processes while ensuring adherence to stringent compliance standards across industries, including life sciences,
