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.

Quality Events give you a way to capture everything that takes place in your business, planned or unplanned, that has to be managed for Quality

Manage the correct documentation and batch record management process demonstrating that each product is manufactured according to industry standards and Good Manufacturing Practices (GMP). Empower