Clinical trials
For all its medical, financial, legal and technological complexity, clinical trials have one primary objective: to lead to the registration of an effective and safe medication.
Investigators Brochure
Based on the Investigators Brochure, we will personalise the entire system and you will give the tools to the entire research team.
Quick and simple.
Data from the patient
Using the Electronic Diary, patients can securely share data with the research team.
This allows the doctor to know what is happening with his patients, how they are reacting to the medicine and whether they are satisfied with the results.
Intuitive and scripted visit model
eOStm provides researchers with the ability to manage medical records transparently and securely.
Our system makes their work comfortable and automates the visit process.
Data flows faster and researchers do not waste their working time.
Randomisation and blinding of medications
Using modern randomisation modules, we ensure full control and safe blinding of the research substance.
With eOStm, you can also track the history of a medicine and manage its distribution.
Full control over the course of the research
Case Report Forms, Informed Consent Forms, contracts and invoices all this and more in one system, always at your fingertips.
One tool that combines appointment schedules and scripts, task lists for patients, doctors and researchers.
Dynamic creation of analyses and reports
With dynamically created analyses and medical reports, the system provides the ability to quickly and efficiently verify key research data.
Security and FDA compliant change tracking module
Every change to eOStm is monitored by Audit Trial mechanisms, making it compliant with medical systems requirements adopted by the FDA.
You will absolutely not miss anything.
Patient
Full control of the treatment during the clinical trial.
Reduced number of visits
Fewer face-to-face visits and better communication with the doctor
Everything in one place
Data on your medical history, the course of your visits and your doctor's recommendations in one place
Clear plan
An integrated, clear and readable medical action plan
Monitoring of health status
Monitoring of the patient's health at home
Important reminders
Generation of alerts and notifications e.g. reminder to take medication
Continuous analysis of results
Analysis of health results based on measurement history and set indicators
Doctor / Researcher
Less paperwork in clinical trials.
Intuitive visit model
An intuitive and scripted visit management model that enables greater automation of the entire operation
Complete documentation
Complete and compliant medical documentation according to the Investigator's Brochure in one structured place
Deviation reporting
Automatic reporting of protocol deviations
Schedule of dates
Schedule management of key dates
Simple communication
Simple communication with other members of the research team
Real-time management
Real-time monitoring and management of each stage of the research
Clinical Research Associate
Safe administration in clinical trials.
Monitoring of changes
Intuitive and clear interface to control changes in the scope of the research
Randomisation of clinical trials
Management of randomisation of the clinical trial according to the accepted research protocol
Configuration of statistics and analyses
Configure any medical statistics and reports related to the clinical trial process
Dynamic analyses and reports
Dynamic creation of analyses and reports based on collected data
Data security
Data security (physical, system, legal and logical)
Monitoring of medicines storage
Monitoring the stock of medical research substance in one system
Sponsor
Process automation in clinical trials.
Several projects at once
Managing several projects and large patient groups from one system
Key notifications
Grouping notifications and personalising their settings
Deviation reporting
Automatic reporting of protocol deviations
Reduced patient drop-outs
Improved patient retention
Forwarding and management of medication distribution
Dynamic creation of analyses and reports based on collected data
Digital project management
Change tracking module according to FDA guidelines - Audit Trial
Check the offer
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