Development of a module to support GMP processes and pass production audits
We are pleased to announce that we have completed the development of a new software module “Register of Pharmaceutical Production Equipment and Systems DSBase-PER” to support GMP processes and production audits.
The DSBase-PER module, through digitalization, improves the quality of management of accounting, operation, maintenance and repair processes of production equipment and enterprise systems, allows you to maintain equipment accounting data, its passport data and technical specifications, operating and repair instructions, logs of operating hours, work performed and malfunctions, information on functional checks.
A single protected and duplicated database of production and technical indicators of equipment provides a significant reduction in the time for searching and obtaining data and increases the efficiency of using staff working time.
This functionality allows you to significantly save transfer time and minimize the labor intensity of these operations for the pharmaceutical company’s personnel.
You can get more detailed information by contacting us.
We sincerely believe that our developments will be not only effective and useful for you, but also easy to use!
Other News
New Release: eCTD-RIMS Version 4.0 with Enhanced Functionality and Intelligent Assistant eCTD-AI
On June 10, 2025, iRIS Soft officially launched version 4.0 of its flagship software — the Electronic Dossier Management System eCTD-RIMS. The update brings a series of significant enhancements and new modules that substantially extend the system’s capabilities for applicants submitting electronic Common Technical Documents (eCTD). Key Updates in eCTD-RIMS Version 4.0: eCTD-Manager – for […]
eCTD in Ukraine: A New Format for Registration Dossiers and Practical Aspects of Implementation
On August 18, a landmark event took place in the regulatory sphere: Ukraine officially transitioned to the electronic Common Technical Document (eCTD) format. From this date forward, registration dossiers for new marketing authorizations must be submitted exclusively in electronic format, with the exception of procedures regulated by Orders of the Ministry of Health of Ukraine […]