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Data-driven Submission Management

Drive faster time-to-market and greater precision by reusing controlled data across global submission processes to simplify work.

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RIM on the CARA Life Sciences Platform™ provides a powerful foundation of regulatory information, managing data to make it easy to identify and re-use across the organisation. This consistent global information flows in and out of your processes, making you more efficient.

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Applications & Registrations

As part of your new regulatory Event or Activity process, Applications are created, leading ultimately to Authorisations /  Registrations, with automated status tracking along the way. This means you can quickly see the global progress of your products to market.

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Submission Planning & Tracking

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.

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Events, Activities & Commitments

Get instant oversight into what has been submitted and where with CARA’s ‘Current Approved’ and ‘Where Used’ views. Automated relationships ensure a smart web of content, submissions and plans to provide instant oversight.

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Product Information Management

Data is the core driver of consistent content, planning, tracking, efficiency, and automation. In short, seamless information flow improves everything. CARA distributes and oulls approved information, balancing regulatory compliance with everyday work.

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Health Authority Corrrespondence

Process communications faster and more consistently with automations to ingest and manage correspondence. Automations make every step more efficient, with translations and workflows bringing order to your processes.

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