Presenting Electronic Equipment Logbook, complying with 21 CFR Part 11 requirements, a simple yet controlled platform for all Pharmaceutical manufacturing to manage logbooks, digitally.
Complying with GMP guidelines, Electronic Equipment Logbook provides capability of defining workflow, SOPs on areas or equipment and building validation control points. Intelligence in system alerts in case there is a deviation from laid procedures, thus saves huge cost and efforts in production environment.
Being a digital platform, it eliminates use of paper logs and further provides analytics for operational efficiency improvements. Analytics gives a multi-dimensional insight on downtime, efficiencies, skills and various other attributes.