CTMS
AMEDON CTMS – Your clinical trial compass
You have to manage one or more clinical trials with associated staff, ToDos, milestones and reports? You would like to have a central place to overview and manage all activities? The AMEDON clinical trial management system (CTMS) supports your workflows and stores your data securely and easily accessible in one system. Get data from all of your eCRFs for management reviews, find your contact persons for an appointment or oversee the TMF documentation.
Our CTMS supports your daily processes for study management and is the key system for your leading staff. That’s why it is configurable for your processes based on the well-established pathways.
The scalable solution fits to small as well as international diversified studies and companies. Via your direct contact to our staff, we will define your best choice.
Complexity reduction
The CTMS is a customizable suite for CROs and sponsors to support clinical study management from internal study approval to TMF check.
Involved staff may work together on one database and in the same workflows on the given tasks.
The CTMS includes as much as possible automatically transferred data from your systems and also offers options for decentralized data capture.
Goal: Central visualization of trial status on different levels (study, country, site), presenting required and important information for management staff and decision makers.
Your Benefit
The M.A.R.C.O. CTMS supports your daily processes for study management and is the key system for your leading staff. That’s why it is configurable for your processes based on the well-established pathways.
The scalable solution fits to small as well as international diversified studies and companies. Via your direct contact to our staff, we will define your best choice.
Our CTMS can be used as part of our other eSolutions or incorporated with applications of other providers like other eCRFs or included in your established IT landscape.
Classic Modules
Study registry
Register new studies in your company and describe relevant key facts for internal overview and announcements.
Medical review process
Decide about new studies based on relevant documentation and track status.
Study overview & management
View and administer study key facts, milestones and timelines, staff and contacts for ongoing studies.
Visit reports
Create, review and approve visit reports for different time points during clinical trials with configurable content depending on the type of trial, the country etc.
Contact management
Full contact database for your trials with role definitions and links to system users to manage privileges in the system.
Document tracking
Compare available versus necessary essential documents for the TMF based on study type and regulatory needs.
eCRF integration
Direct transfer of relevant eCRF data to your overviews.
Data Warehouse integration
Direct connection to AMEDON Data Warehouse to create live or static reports on your data. Visualize reports in CTMS for different user groups.
We would be happy to answer your questions about our services personally.