Are you interested in how you can optimize your impurity analysis workflows to obtain greater productivity, sensitivity, accuracy and reproducibility to meet increasing regulatory requirements and lower limits of detection? Would you like to achieve all of this, whilst also increasing laboratory efficiency and reducing the cost per sample? If so, then you will find our four pharmaceutical impurity on-demand webinars, delivered by experts from LGC Standards, Thermo Fisher Scientific and Broughton Laboratories, valuable.
On-demand webinars:
| Overview of Pharmaceutical Impurities and Reference Standards |
| Inorganic Impurity Analysis Workflows |
| Organic Impurity Analysis Workflows |
| Broughton Laboratories Case Studies on Pharmaceutical Impurities |
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Additional resources
To supplement the webinars, why not take a look at these articles related to the webinar topics above:
- Introduction to Pharmaceutical Impurities: An Interview with Dr. Christian Zeine ›
- Top Four Questions About Pharmaceutical Impurities ›
- Five Additional Pharmaceutical Impurity Questions ›
