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.
eTMF Archive
CARA’s eTMF Archive gives you a better way to manage critical trial documentation – from first file to final archive.
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
Getting Value from AI : Why Life Sciences Companies Can’t Afford to Waste Time
Artificial intelligence is everywhere. Every week seems to bring another announcement promising smarter summarisation, faster drafting, or a new assistant that can shave seconds off
Turning Internal Knowledge into AI Intelligence: Why Context Is Everything
The Hidden Cost of Deploying AI Without Context There is a quiet assumption embedded in most conversations about AI adoption that deploying a large language
The Prompt Problem: Why Uncontrolled AI Inputs Are a Compliance Risk
When AI Inputs Become a Compliance Liability When organisations evaluate AI tools, the conversation usually centres on model capability: accuracy, speed, hallucination rates. These matter.
