Systems for pharmaceutical development

gRIS FAMILY

 

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.

moduleGRIS DEVELOPMENTGRIS REGISTRATIONGRIS TRANSFER
project management
RA
transfer management
portfolio management
patent analysis
trademark module
launch module
affiliates
SC
tasks
controlling & reports
audits
GGD
budget
capacity
timeline
market
subprojects
timesheets
documents
emails
ITA
project diary
sandboxing
country scopes

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.

DMS

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.

Samples Diary

Planning, analysis and evaluation of laboratory tests considering the specifics of
pharmaceutical research.

Whitebook

A system for displaying the data structure of projects from other systems in the form
of dynamic maps.