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

Deal with incoming Medical Inquiries and information requests via call centres, emails, and more. Real-time searching for answers, including automatic sending, and full per-country data

Ensure the data in your CARA Life Sciences Platform meets the standards and norms of the MedDRA dictionary / thesaurus.  

Revolutionise clinical trial management with an integrated eTMF on the CARA Life Sciences Platform. Our eTMF solution offers comprehensive, DIA reference-model based documentation management, automated

Consolidate physical mail and email with the CARA Platform. Our Digital Mailroom provides a comprehensive solution for adding workflows, out of office features, and delegating

CARA for Quality Management is a configuration package with functionality for managing Quality documentation as well as Quality Events, CAPA, Change Requests, and Quality Evaluations.