Make the clinical studies at your hospital more efficient with our management system.
A comprehensive web-based solution for hospitals and affiliated centres that want to efficiently monitor and supervise ongoing clinical studies at their facilities.
The application allows hospitals to collect and manage all the information related to ongoing clinical studies.
Accessible to administrative staff or researchers, the database provides essential support to keep track of all important information associated with clinical studies, offering an accurate and detailed view of the current situation.
Accessible to administrative staff or researchers, the database provides essential support to keep track of all important information associated with clinical studies, offering an accurate and detailed view of the current situation.
Our solution
Advantages
REAL-TIME DATA
We value strong and enduring partnerships with our clients, built on human relationships, to achieve mutual success.
OPTIMIZED WORKFLOW
We prioritize our clients' unique needs and goals, ensuring they are at the heart of our strategies and proposed solutions.
ADMINISTRATIVE STATUS MONITORING
We conduct ourselves with the utmost integrity, maintaining transparency and ethical practices in all our interactions.
Key features
The system offers advanced search functionality that allows personalized searches across various fields. This enables quick identification of desired clinical studies and obtaining an accurate overview of the data.
CUSTOMIZED SEARCHES
For each clinical study, it is possible to track all administrative activities, adverse event reports (SAEs), amendments, and recruited patients. This allows monitoring the progress and progression of each study or conducting more general analysis.
ACTIVITY MONITORING
The system gathers all administrative information for each clinical study, including protocols, drugs, study types, sponsors, involved facilities, lead researchers, departments, and all other relevant data such as study start and end dates, ethical committee and regulatory approval, and different study phases.
The system allows uploading document templates to facilitate automatic creation of study management documentation. Templates can be customized.
COMPLETE DATABASE
DOCUMENT TEMPLATE UPLOAD
The system allows exporting reports with all the information regarding individual clinical studies or an entire set of studies. These reports provide detailed analysis of aggregated data and trends in ongoing clinical studies. Reports can be customized according to specific needs.
The system supports different permissions and access levels for users. Specific roles and appropriate permissions can be assigned to each user, ensuring they only have access to relevant functionalities and data for their role.
CUSTOMIZED REPORTS
USER MANAGEMENT
Designed to accommodate the evolving needs of organizations handling multiple trials. It can integrate with regulatory submission platforms allowing for direct transfer of trial documents.
INTUITIVE USER EXPERIENCE
With our user-friendly web-based application, you can effortlessly monitor the administrative status of various clinical studies, distinguishing between ongoing and completed studies, and highlighting any essential missing documents.
Our goal is to simplify and optimize the administrative management of clinical studies, allowing you to focus on delivering valuable healthcare services while maintaining strict oversight and compliance.
Our goal is to simplify and optimize the administrative management of clinical studies, allowing you to focus on delivering valuable healthcare services while maintaining strict oversight and compliance.
© 2024 Promeditec Innovation S.r.l.
Via dell'Orologio, 6
34121 Trieste
(+39) 040 2457504
info@promeditec.com
Via dell'Orologio, 6
34121 Trieste
(+39) 040 2457504
info@promeditec.com