To guarantee the safety and efficacy of products manufactured in cleanroom environments, organizations such as International Organization for Standardization (ISO) and regulatory bodies such as the ...

To meet the requirements of regulatory agencies, pharmaceutical products are produced in a controlled setting. One example of such a controlled environment is a cleanroom, which is used to minimize ...

Understanding the Requirements for Particle Monitoring in Pharmaceutical Cleanrooms begins with a grasp of the current regulations. The current international standards for defining contamination ...

Rotronic’s new CRP5 cleanroom panel is fitted with a diaphragm sensor and validated according to good manufacturing practices (GMP) directives. The panel is suitable in situations when a high-degree ...

Rotronic’s cleanroom panel CRP5 is fitted with a diaphragm sensor and validated according to good manufacturing practice (GMP) directives. The device has been specifically designed for applications in ...

Biopharmaceutical manufacturing relies on many advanced technologies. Still, many pharma companies have room to improve when it comes to taking full advantage of everything modern tech has to offer.