Specialized modules

Adverse events

The module is intended for recording events or circumstances that could have resulted or did result in avoidable physical harm to a patient.

The list of possible event types is given in the taxonomy code list, which is based on the currently valid methodological material of the Adverse Event Reporting System (SHNU).

The module is able to ensure records and processing procedures according to a user-defined sequence of activities.

Clinical studies

For healthcare facilities participating in clinical trials (commercial/academic), we offer a Module supporting the management of their own clinical trial agenda and the recording of its documentation and evaluation of the treatment of patients included in any of the clinical trials as assigned by external entities in all their phases.

• patient recruitment
• Recruitment completed, treatment and monitoring of patients continues
• termination, archiving of CS (terminated CS)

Based on regulations (within the framework of the Clinical Trials, activities are regulated and regulated primarily by the Act on Pharmaceuticals 378/2007 Coll., the Decree on Good Clinical Practice No. 226/2008 Coll., and also Good Clinical Practice (GCP), contracts with sponsors and continuously monitored by external monitors (Clinical Research Associate), the clinical studies module provides support for the following key activities:

• selection
• preparation
• implementation
• coordination
• data collection and entry
• monitoring
• audits
• archiving of clinical studies

For example, reliable identification of cancer is of great importance not only from a societal perspective, but also from a medical and scientific perspective. It offers precise epidemiological data that can be the basis for effective preventive measures. "From a professional perspective, it provides the opportunity to record in a concise form an accurate description of the extent of the tumor, a classification of its characteristic features, i.e. information necessary for choosing the optimal treatment and for comparing therapeutic results from different workplaces." ("International Classification of Diseases for Oncology")

Oncology department.

• 24/7 service support
• Favorable price
• Validation for each released version
• Company certification ISO 9001:2015
• Company certification ISO 27001:2013
• ISBT 128 certification
• Professional user support
• Open options in customizing the program to the user
• 30 years of experience in healthcare software development