Resource Hub

The CARA Life Sciences Platform supports the ongoing task of distributing safety information on a periodic basis to affiliates, distributors, and other third parties responsible for safety reporting to NCAs and tracking interactions.  

CARA provides comprehensive support for both image and video formats, enabling users to collaboratively review materials, share them with colleagues, and publish content seamlessly within the platform.  

Managing complaints is not just a regulatory requirement but impacts the public image of your company. The CARA Life Sciences Platform allows you to ensure that complaints are quickly and automatically routed on workflows and escalations through to the resolution.  

Training and certifying employees in the same system as the documents themselves ensures a seamless experience with greater oversight. The CARA Life Sciences Platform provides the ability to define courses, roles and curricula for such content, but also to log – and generate training certificates for – any external training,

The CARA Life Sciences Platform offers a unified and traceable way to create and distribute Risk Management Plans and associated documents to Affiliates and Distributors. Traditionally, this process would involve multiple external systems – one for sharing content and another for registering and reporting on implementation status. With the CARA

Quality Documents Management on the CARA Life Sciences Platform provides a modern, central DMS for all types of Quality documentation. Beyond the standard functionality of content creation, review, and approval, CARA supports publishing, training, eSignature, controlled printing, and site-control to support enterprise needs.  

Managing the PSMF is a complex, ongoing task, involving the updating of sections owned by different parts of the business, and particularly the creation of Annexes from information that comes from various sources. The CARA Life Sciences Platform facilitates the entire process, including the automatic generation of Annexes.  

It is a legally mandated obligation for each pharma company to track PV agreements and contracts relating to pharmaceutical products and the exchange of Adverse Events. Rather than being a requirement that can be met by a stand-alone contracts management system, this requirement is more complex. The CARA Life Sciences