Experts from the USP and the European Pharmacopoeia delve into some of the real-world challenges they face when developing pharmacopoeial reference standards and discuss the solutions they deploy to ensure they are robust.
The speakers share practical knowledge from detailed case studies that will improve participants’ understanding of best practices to ensure the highest quality and consistency in pharmaceuticals.
Target audience
This webinar is of interest to professionals from the pharmaceutical industry (analysts, laboratory scientists/technicians, QC/QA managers, regulatory affairs staff) and from organisations providing a contract laboratory service.
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