
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

Cytonics Selects CARA Life Sciences Platform for Rapid eTMF System Implementation
Cytonics, a biotechnology research and development company specializing in diagnostics and therapeutics for osteoarthritis, has selected Generis, the provider of the AI-enabled CARA Life Sciences

Kwizda Pharma Adopts CARA Life Sciences Platform for Rapid QMS Implementation with Minimal IT Resources
Kwizda Pharma, a division of Kwizda Holding GmbH and a leader in the Austrian healthcare market, has selected the CARA Life Sciences Platform from Generis,

eTMF Archive on the CARA Life Sciences Platform
eTMF Archive on the CARA Life Sciences Platform The CARA Life Sciences Platform offers a comprehensive Electronic Trial Master File (eTMF) Archive, designed to enhance
