The university plays a vital role in addressing social challenges and improving quality of life. Its success is built on five dynamic institutes specializing in chemistry and biotechnology, food and ...

In the pharmaceuticals sector, a primary objective of regulatory guidelines is to maintain control over contamination and preserve the sterility of products manufactured within a pharmaceutical ...

In crucial areas, the majority of the recent regulations promote the use of continuous viable air monitoring. The BioCapt ® Single-Use (BCSU) Cleanroom Microbial Monitor by Particle Measuring Systems ...

The mass production of pharmaceuticals has significantly evolved since the industrial fabrication of synthetic drugs towards the end of the 19 th century 1 with efficient developments in process ...

One of the main goals of pharmaceutical regulatory rules is to keep environmental contamination at a minimum. According to the EU GMP Annex 1 regulatory standard for sterile drug products, a ...

Editor’s note: This article is the third in a series to help practitioners learn about the AICPA’s new quality management standards and prepare to implement them. The new final standards on quality ...

In this free webinar, see how environmental monitoring in pharma supports contamination control, inspection readiness and a demonstrable state of control. Attendees will learn how to design a ...