Validation and Calibration Software de ELLAB - VALSUITE

Intuitive software on a single platform that allows you to work with traditional systems with thermocouples and dataloggers. Guarantees traceability and data integration in compliance with FDA 21 CFR Part 11. "Ellab Monitoring Solutions" complies with GxP, HACCP, EU GMP annex 11 guidelines and ISO 22000 food standards.

Software allows custom configuration of all reports - reports with total security that none of the data could have been modified and ensuring "Data Integrity" and is summarized in:         

• Clear "PASS / FAIL" criteria
•  "Cold and Hot Spots" obtention.
• Specific requirements based on current regulations, EN17665 (EN554), EN 13060, EN285 ...
• Reports or validation reports: Limits report, Fo,Po lethality reports, Statistical reports, calibrations, ...
• 3D analysis - obtaining demonstrative videos of the thermal procedure
• Data Integrity (compatible with Windows Security, Electronic Signature, Audit Trail,...

Developed to offer maximum flexibility and control over data and events, EMS has significantly evolved how, where and when data can be viewed and managed across the broadest spectrum of clients, from single/user to multiple locations/users. EMS also has reporting options to meet the simplest and most complex customer requirements.          

• Access to data in real time 24/7.
• Management and immediate communication via E-mail and SMS - interactive notifications.
• Access to information locally PC, intranet or network - internet.
• Interactive access to the plant synoptic, tables, graphs and data analysis.
• Studies of the distribution of the cold chain - product transport.
• Thermal distribution studies - Mapping.
• Monitoring of relative humidity, temperature, LUX in drying and smoking processes, etc.
•  Food Quality and Safety.
• Easily demonstrate that control and monitoring equipment is available in all critical areas.
• Demonstrate that the equipment measures precisely and accurately.
• Management of alarms and established critical limits.
• Generation of automatic reports correlated with each of the manufacturing batches.
• Production of Audit Trails with corrective notes for the audits.