Clinical Without Boundaries
Clinical Trial Management System (CTMS)
Electronic Trial Master File (eTMF)
Medical Writing
Clinical Trial Management System (CTMS)
Manage Clinical Trials from Protocol Approval to the Study Closeout through an integrated CTMS on the CARA Life Sciences Platform™. CTMS enables the consistent use of the Study Protocol and Study Master Data along the entire Clinical Trial operations value chain.
Electronic Trial Master File (eTMF)
Our eTMF module provides DIA-reference model-based management of the documentation for trials, with missing document reports, automations for site and trial setup and an investigator or site portal. All based on a single information lake, our eTMF system is seamlessly connected to CTMS.
Medical Writing
The CARA Life Sciences Platform includes data-to-document tools to automatically generate Clinical Protocols and Study Reports, and then edit those documents using Structured Content Authoring (Component-based Authoring).
Latest Resources
True Connectivity: The Lifecycle of a Drug in the CARA Life Sciences Platform
With today’s need for speed and efficiency in the life sciences industry, Regulatory Affairs, Pharmacovigilance, Clinical Research, and Quality Management cannot operate as independent islands
Barry – The Story of a Drug in CARA Life Sciences
Gone are the days when Regulatory Affairs, Pharmacovigilance, Clinical Research, and Quality Management could operate as independent islands within a pharmaceutical organisation. With todays need
Digital Mailroom on the CARA Life Sciences Platform
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
