Pharmaceutical manufacturers are required to requalify their production facilities annually in accordance with GMP requirements. During steam sterilization, all critical points must be monitored: extensive piping systems, installed components such as …

A pharmaceutical company was faced with the challenge of carrying out several autoclave validation runs at short notice. Its own pool of validation equipment was already fully utilized, while the project still had to be completed on time and in full…

As part of a mapping study, a pharmaceutical solid storage warehouse was evaluated to verify that climatic conditions remained reliably within the defined limits even during particularly warm months. For this project, a total of 46 EBI 300TE data loggers…

A baby food manufacturer was faced with a critical challenge: during the sterilization of baby food jars in an autoclave, unexplained pressure fluctuations occurred. Initial assumptions pointed to issues with pallet stacking, but the root cause could not…