Applications & Registrations
Tracking applications and registrations is a core mission of a complete RIM system. CARA takes this further by tying application and authorisation information to your submission structures and even down to individual documents. This means you are never more than one click away from complete context.
What is applied or authorised where?
RIM on the CARA Life Sciences Platform enables tracking and maintenance of Applications and Registrations (also known as Authorisations). As part of your new regulatory Event or Activity process, Applications are created, leading ultimately to Registrations, with automated status tracking along the way. This means you can quickly see the global progress of your products to market.
Leverage an interconnected web of documents and data
Traceability is key in our RIM system, allowing you to immediately identify which medicinal products are approved and which documents are related to that registration. Our traceability is always bi-directional, enabling you to view the relationship from the registration, the medicinal product, the document, or any other related object.
See the best of regulatory content management with Submission documents on the CARA Life Sciences Platform