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Rapid Viable Monitoring and Regulations for Pharmaceutical Manufacturers

New monitoring methods for viable contamination are now given extra consideration by regulatory bodies with the trend leading away from traditional settle plates. In this blog series we discuss the regulations involved and the aspects of implementing new methods for better, quantitative data.

Newsmonitoramento de partículas

Requisitos de Monitoramento de Partículas em Salas Limpas Farmacêuticas

Pharmaceutical manufacturers must demonstrate compliance with the regulations at every stage before a drug can be released to market. To satisfy these requirements, the products are manufactured in a controlled environment, known as a cleanroom. A cleanroom is the fundamental starting point for contamination control.

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