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
Сompletion of the development of the new Digital Medical Device Quality System eMDD-RIMS
We announce the completion of the development of the new Digital Medical Device Quality System eMDD-RIMS. eMDD-RIMS is a document management system for manufacturers, authorized representatives and distributors of medical devices that significantly simplifies the management of regulatory and quality documentation. The system allows you to create a centralized documentation repository with access for all […]
New Release of the Electronic Dossier Management System eCTD-RIMS
iRIS Soft has completed the development of a new release of the Electronic Dossier Management System eCTD-RIMS. The new version incorporates user suggestions for improving system efficiency, as well as experience accumulated during system operation and submission of eCTD documents to the Applicant’s Cabinet of the State Expert Center of the Ministry of Health of […]