Errors and deviations occur in every manufacturing process. But when they happen in pharmaceutical industry, it means that people suffering from life-altering diseases may not receive their medicine in time or not in the expected quality.
A typical area – which is often neglected – where errors and deviations occur, is the process of defining and setting the production parameters on the process equipment. In most pharmaceutical manufacturing sites, this process involves numerous activities of which many are performed manually and on paper (e.g. review and sign-off, versioning, storing, parameter inputting) – all while we know how such way of working exposes manufacturers to high risks for errors…
The most effective remedy to mitigate such risks is digitization. By digitizing the defining and setting of production parameters, the process becomes bulletproof and error-free, ensuring that the patients get their much needed, high-quality medicines on time, every time.
The advanced solution for the digitization of the production parameters’ life-cycle is MePIS RM – discover more
