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LiveDOK for pharmaceutical companies

Always knowing what’s what

The operating of process plants in the pharmaceutical industry has very special documentation requirements. Numerous regulations of various health authorities have to be observed, and stringent qualification and validation processes according to EU-GMP guidelines need to be complied with. So for plant operators, drawing up and maintaining plant documentation absorbs great resources in terms of time and personnel, especially after production plants have been newly installed, modified or extended. Indeed, in order to get manufacturing or operating permission, any discrepancy between submitted plans and documents on the one hand, and actual realization in the plant on the other, has to be completely ruled out. The conditions for fulfilling this requirement are not favorable: speedy execution of documentation tasks is often hampered by a wide assortment of data formats and end devices, often still in conjunction with existing piles of paperwork.

LiveDOK by RÖSBERG greatly simplifies dealing with documents, frees up resources and ensures consistent quality. At the same time, the software solution improves your use of planned downtimes and simplifies maintenance, along with many other benefits.


Up-to-date, legally compliant documentation

Your process plants change in the course of time. Extension, modernization and other adaptations often deviate from the original planning documents drawn up for the purpose.