Betrieb und technische Betreuung von ProzeÃleitsystemen in der pharmazeutischen IndustrieAktuelle Ergebnisse aus dem GemeinschaftsausschuÃ âValidierung von ProzeÃleitsystemenâ von NAMUR (Interessengemeinschaft ProzeÃleittechnik der chemischen und pharmazeutischen Industrie) und GMA (VDI / VDE-Gesellschaft fÃ¼r MeÃ- und Automatisierungstechnik)
Volker Teuchert Centeon Pharma GmbH, Marburg/Lahn
Operation and Maintenance of Process Control Systems in the Pharmaceutical industry / Results of the joint committee âValidation of process control systemsâ of NAMUR and GMA
After successful completion of a prospective GMP compliant validation the automated system including the process control system is being released for production. During its following use in operation the validated status of the system needs to be maintained through qualified operation and technical support. For example, the systemâs technical documentation has to be updated contemporaneously in case of changes, access regulations have to be implemented and adapted to varying users, backup and archiving of data and software has to be assured, new users must be trained. The execution of these measures is written down in Standard Operation Procedures (SOPs). To assure a reproducible execution regardless of individual working methods of different persons, an appropriate organisation has to make sure that the SOPs are being followed. This also includes documented training on the contents of the SOPs. The article provides a survey of the results of the joint committee âValidation of process control systemsâ of NAMUR (Standardisation Association for Measurement and Control in Process Industries) and GMA (Society for Measurement and Automatic control of VDI (German Association of Engineers) and VDE (German Association of Electrical Engineers)) on this area of work.
Key words Instandhaltung Â· Pharmaproduktion Â· ProzeÃleitsysteme Â· Standard Operation Procedure (SOP) Â· Validierung
Â© ECV- Editio Cantor Verlag (Germany) 1999
pharmind 1999, Nr. 9, Seite 858