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Clinical Solutions Template
Modern Content Management
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.
- Quality Documents Management
- Quality Events
- Corrective and Preventive Actions (CAPAs)
- Change Controls
- Deviations
Benefits
A modern interface makes the CARA Life Sciences Platform easy to use and personalised to the user’s work
Users who work across multiple parts of the business can have access to all use cases on the same platform
Data and content can flow between any solution on the platform without integration, enabling seamless collaboration, discovery, and traceability across the business.
The UI is common between all business processes, reducing training and improving adoption.
Applications & Registrations
Document creation, review, and approval with eSignature, periodic review, and effectiveness, and controlled printing. Video also supported
Applications & Registrations
Document creation, review, and approval with eSignature, periodic review, and effectiveness, and controlled printing. Video also supported
Applications & Registrations
Document creation, review, and approval with eSignature, periodic review, and effectiveness, and controlled printing. Video also supported
What is MedDRA?
A subscription-based product of the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH)
Why is it used?
Provides a rich and highly specific standardised medical terminology to facilitate sharing of regulatory information internationally for medical products used by humans
How will we use it?
By integrating the CARA platform with governed and regulated dictionaries from MedDRA, CARA LifeScience products will provide internationally standardised terms in the regulated industry. These terms would be used in registration, documentation and safety monitoring of medical products both before and after a product has been authorised for sale. This includes all applications in pharmaceuticals, biologics, vaccines and drug-device combination products
Document creation, review, and approval with eSignature, periodic review, and effectiveness, and controlled printing. Video also supported
Users who work across multiple parts of the business can have access to all use cases on the same platform
Data and content can flow between any solution on the platform without integration, enabling seamless collaboration, discovery, and traceability across the business.
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