Boosting your data integrity with MES
The usage of an electronic manufacturing execution system (MES) like Werum’s PAS-X enables pharmaceutical and biotech manufacturers to fulfill data integrity requirements. For instance, audit trails in an electronic system make it obvious who created a record, when it was created, who made a change, when the change was made, and the reason a change was made. An MES automatically tracks this information: Data is attributable to a unique user with a secure password and role-based permissions, preventing changes from being made by unauthorized users.
Another example is that the use of an MES enables pharma companies to have less human interventions, which reduces the chances of human errors. And it has interfaces to other systems to automatically fetch values of activities. This way, the system ensures that the data fetched or pulled from surrounding systems is correct. Audit trails and batch reports are functionalities, which enable manufacturers to review everything so that they can ensure that data recorded is truthful.
With this key role, using an MES will boost your data integrity compliance and process quality, since your data is attributable, legible, contemporaneous, original and accurate!