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The Kronus Clinical Trial Management System (CTMS), offers a FDA-validated solution with everything you need in one package, including worksheets, documents, calendars, contacts, schedules, payments, milestones, and more, all while ensuring compliance. Some of the main features of the platform include, but are not limited to: MASTER DATA MANAGEMENT: Centralised interface for defining and managing lookup tables, such as doctors, sites, sponsors, regulators, and IRB, simplifying data management. DOCUMENT MANAGEMENT COMPLIANCE (eTMF / eISF): Maintain FDA-validated structures for Trial Master Files and Investigator Site Files, with controlled access and meticulous audit tracking. PATIENT SCHEDULING: With this module you have a single interface where you can management the entire calendar of a research centre, split across multiple subjects, multiple studies and multiple subject visits.
Provider
nuvoteQ
Located In
South Africa
Open API
Yes
Deployment
Cloud, SaaS, Web-Based
Training
In Person, Live Online, Webinars, Documentation, Videos
Support
Email/Help Desk, FAQs/Forum, Knowledge Base, Phone Support, 24/7 (Live rep), Chat
- Research Clinics / Hospitals - Contract Research Organizations (CROs) - Biotech and Pharma Companies
Content Source: Kronus
Green rating bars show the winning product based on the average rating and number of reviews.
Kronus Reviews
"Versatile and User-Friendly Learning Management System"
Overall: Having sampled other learning management systems, Kronus stands head and shoulders above the rest.
Pros: Exceptional support - both in terms of migrating training data from our previous learning platform, and in terms of setup and training to use Kronus. The software itself is also a pleasure to use and manage, with a lot of flexibility in terms of accommodated training formats.
Cons: The inability to add and remove users as an administrator - this needs to be done via the Nuvoteq team. It is a minor issue though, as the team is responsive and actions access requests promptly.
