Watch our quick learning and learn in only 10 minutes what key challenges manufacturers are facing when selecting media for media fill tests and how to overcome them.
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Former MHRA inspector Rachel Carmichael discusses outsourcing areas of your quality system including what would drive this decision, aspects of the operation that can be supported and measures to facilitate the process
Pharmaceutical process development involves multi-disciplinary groups of chemists and analysts whose goal it is to create the API by the cheapest, most efficient route while ensuring product safety through effective impurity control measures.
If you are currently involved in high throughput (HT)/parallel synthesis, looking to improve automation productivity gains, or considering investments in automation; don't miss this webinar!
In this webinar, Lynne Byers explains how you can continue to keep your manufacturing site operating compliantly with significantly less staff.
Essential points of active air sampling units for use in your high-grade cleanrooms, along with requirements for prevention of cross-contamination.
This webinar will address the evaluation of microbiological, environmental monitoring data as well as what would be considered significant differences in data.
Stability testing is a vital part of product development and is conducted throughout a product’s life cycle.
TOC analysis in the lab, at-line, or online enables efficiency gains and process understanding for cleaning validation and monitoring programs.
Save time and ensure your titration data is accurately recorded to the titrator with Supelco® SmartChemicals.