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

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

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