In the pharmaceutical industry the requirements regarding process safety are higher than in other industries, e.g. the GMP (Good Manufacturing Practice, introduced by the FDA in 1962) in the regulated environment which makes great demands on the software producer as well as on the pharmaceutical industry regarding compliance of IT systems. Thus a lot of companies tend to refrain from increasing the necessary ratio potential by a reinforced use of IT Support or to raising their revision and compliance safety respectively, although e.g. in the field of Digital shift books the research demand could be reduced by more than 90% when using New Solutions Finito.
When operating machines and plants, events occur that must be documented in writing in shift books together with the measures taken. In a large number of companies this is being done and has been done by paperwork.
The digital shift book Finito will make handwritten shift logs redundant and provide a company-wide homogenous recording of information and instructions. All information gained will be stored revision-safe in a centralized data base. This way up to 90% of the time needed can be saved e.g. when doing research.
The digital recording of shift messages allows a swift statistic evaluation. Malfunctions and errors at machines and plants can be detected manually and - as far as technically possible - also be documented automatically which is of essential significance when it comes to flow manufacturing processes.
Accumulated data will be directly taken over in the electronic shift book Finito and serve as a basis for individual reports as well as a knowledge data base for troubleshooting or optimizing work flows and safety measures.
A comprehensive configuration module for administrating reports, shift times and user rights makes Finito Digital Shift Book a flexible and highly efficient tool for industrial companies.
Here you can find the advantages of Finito Digital Shift Book and how you can use the shift book in your business in a highly efficient way: