Reg

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

Case Study

Pfizer Case Study

Learn how CARA enabled a global Pharmaceutical company to move away from legacy systems and improve user experience.

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