QUALITY PLUS

QUALITY PLUS is the most popular application in the pharmaceutical sector in Italy. The solutions allow her to reach a new frontier in the management of laboratory activities.

QUALITY PLUS is a highly configurable and conforming to the 21 CFR Part 11 and developed in compliance with the standards of reference, cell, GLP, GAMP

All these features make it a suitable instrument to operate, as well as in the pharmaceutical industries, even those chemicals, food and cosmetic.

The main features of the system are: ease of using A simple interface and user-friendly ensure rapid familiarization with the application. The Windows-like interface enables reduced staff training periods.
Complete definition of the specific QUALITY PLUS allows you to define all the specifications used in laboratories for analysis, complete and accurate products, specifications, methods, wise men, etc.
The analytical certification management system handles punctual so each phase of the analytical certification by inserting the customer request.
The Scadenziari management through the management of the Scadenziari, protocols, the lots and related deadlines is also achieved the stability control.
Management and link the instrumentation all related tools are defined in the system and you can check the status of usability, track usage, and schedule the tasks of maintenance and verification.
The laboratory materials management monitoring of all the materials consumption and the reagents from their input in the laboratory on their use, by registering their consumption.
Evaluation of suppliers we can define a plan of control of suppliers, which varies depending on the results obtained in the preceding controls.
Statistical analysis of historical data QUALITY PLUS allows statistical processing of historical data. Displays products data processing using graphs for an easier understanding.

 

EASY OF USE

Simple and user-friendly interface ensures rapid familiarization with the application. The Windows-like interface allows periods of reduced training of personnel

COMPLETION OF SPECIFICATION

QUALITY PLUS allows you to completely and accurately define all the specifications used in Analysis Laboratories such products, specifications, methods, tests, etc..

MANAGEMENT CERTIFICATION ANALYTICAL

The system runs on time every step of the Analytical Certification, Request for the inclusion of analysis.

STABILITY

Through the management of schedules, protocols, and lots of deadlines, is also made stability control.

INSTRUMENTS MANAGEMENT

All instruments are connected as defined in the system and you can check the status of usability, trace the use and schedule maintenance and verification..

MATERIALS MAGEMENT

The monitoring of all consumables and reagents from arrival in the laboratory to use them, recording all their consumption.

EVALUATION OF SUPPLIER

It 'can define a plan for monitoring of suppliers, which varies depending on the results obtained in previous audits..

STATISTICAL ANALYSIS OF HISTORICAL DATA

QUALITY PLUS allows the statistical analysis of historical data. The data produced by drawing displays graphs for easier understanding.