Systems for pharmaceutical development
gRIS is a specific system for pharmaceutical industry allowing fast access and intuitive interpretation of your data. It covers all the phases of pharmaceutical development from the management of initial ideas, project execution, clinical testing to registration and later manufacturing.
It is divided into three autonomous blocks as depicted bellow, which can be used independently or create one integral solution.
|module||GRIS DEVELOPMENT||GRIS REGISTRATION||GRIS TRANSFER|
|controlling & reports|
Capacity of the Equipment
System for capacity planning of the defined equipment and operators. It enables
automation of the resource planning process and monitors its actual use.
Global Generic Database
The GGD system is integrated with development systems in individual research
centres, and centrally provides information on the global state of the research,
including the possibility to manage this top-level research.
Documentation system for GxP environment
Health, Safety & Environment
HSE allows the management of data regarding the substances used in terms of
occupational safety and environmental protection. Every time you are going to work
with a hazardous substance, you shall be automatically alerted how to handle it.
Planning, analysis and evaluation of laboratory tests considering the specifics of
A system for displaying the data structure of projects from other systems in the form
of dynamic maps.