Purity Requirements and Measurement Technology for Pharmaceutical Gases

This outlines the quality requirements for pharmaceutical gases, how the quality is influenced, and which regulatory guidelines must be considered. We will show you what to pay attention to during production and in distribution systems, as well as what you need to consider during operation, maintenance, and monitoring systems. The qualification process will be discussed, along with the requirements for sterile gases.

The microbiological testing of gases and the use of devices for particle, oil content, dew point, and germ determination will be covered in the workshop, including what to consider when calibrating the devices. Focus on the essentials with the help of risk analyses and achieve GMP compliance through professional risk assessment.