Submission Planning & Tracking
Everything is easier with a repeatable process. CARA provides the tools to create consistent global submission processes, as well as the flexibility to tackle ad-hoc submissions and agency interactions.
Start Prepared
While the triggers for a new submission or regulatory initiative may come from a centralised plan or a health authority request, RIM on the CARA Life Sciences Platform provides a consistent and repeatable process for managing them.
Automate Your Processes
Instead of basing workflows on simple document review and approvals, CARA enables and captures your full business process including decision points, correspondence and meeting minutes. Your process is also guided, with the system providing next steps intelligently based on your type of submission and context.
Act and React Based on Global Knowledge
Throughout your submission processes, CARA provides powerful ‘Where Used’ functionality to instantly identify where any data, content, events, activities and level components might be used. There is also a ‘Current Approved’ view in order to understand what submissions or variants may have gained approval globally. This, along with the out-of-the-box reporting builds a picture over successive submissions to identify corporate and process bottlenecks and improve the timelines and performance from one submission to the next.
Start Prepared
Automate Your Processes
While the triggers for a new submission or regulatory initiative may come from a centralised plan or a health authority request, RIM on the CARA Life Sciences Platform provides a consistent and repeatable process for managing them.
Instead of basing workflows on simple document review and approvals, CARA enables and captures your full business process including decision points, correspondence and meeting minutes. Your process is also guided, with the system providing next steps intelligently based on your type of submission and context.
Act and React Based on Global Knowledge
Throughout your submission processes, CARA provides powerful ‘Where Used’ functionality to instantly identify where any data, content, events, activities and level components might be used. There is also a ‘Current Approved’ view in order to understand what submissions or variants may have gained approval globally. This, along with the out-of-the-box reporting builds a picture over successive submissions to identify corporate and process bottlenecks and improve the timelines and performance from one submission to the next.
Latest Resources
CARA Management Centre – Life Sciences
Consistent configuration across environments The CARA Management Centre (CMC) is a standalone application that connects to your CARA instances via the REST API giving enterprise
The Future of Life Sciences Technology: AI Governance, Information Architecture & Digital Transformation
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CARA 5.15 Feature Release – Deep Export
One action. Every document in place. Every exception accounted for. Moving large volumes of documents is rarely just a technical task. There is usually a
