Fast, accurate analysis of impurities is vital to cost effective pharmaceutical production and to public health. Monitoring must consider bio-availability, toxicity, and the quantity of contaminating elements to be in compliance with global pharmacopeias. ED-XRF is an analytic technique that conforms to recommended analysis processes but without extensive sample prep – reducing time and cost. This paper explains the ED-XRF analysis process and validation procedures, and presents obtainable detection limits.
Antibiotic-resistant bacteria are a growing concern, and with good reason—an estimated 23,000 deaths and two million illnesses occur annually in the U.S.
Pharmaceutical product quality, effectiveness and shelf life depend significantly on the water content in these products. Measuring residual moisture content is important for monitoring process control, specifying samples and optimizing freeze-drying processes for lyophilized products. Key learning objectives:
Understanding the importance of selecting the right KF and sample handling techniques
Implementing Near-IR for moisture analysis in lyophilized and other pharmaceutical products
Quantifying residual moisture online in the drying process
This webinar presents challenges related to environmental work, refers to relevant undesirable effects, and suggests solutions for how they can be eliminated or avoided. As an example methodology, it will discuss using environmental analysis according to the CLP protocol, and cover some available technologies.
The 2015 International Chemical Congress of Pacific Basin Societies (Pacifichem), will take place in Honolulu, Hawaii, USA, December 15-20, 2015. The conference is sponsored jointly by the American Chemical Society (ACS), the Canadian Society for ...