How are pharmacopoeial reference standards characterised? How are assigned values (or purity values) established? How are the quality and reliability of the official reference standards at the EDQM and USP ensured? This webinar provides case studies to demonstrate the importance of orthogonal analytical techniques in chemical structure characterisation, impurity identification and value assignment.
Target audience
This webinar is of interest to professionals from the pharmaceutical industry (analysts, laboratory scientists/technicians, QC/QA managers and regulatory affairs staff) and from organisations that provide contract laboratory services.
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Duration: 43 minutes.
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Other Events/ Training Sessions
- Joint EDQM-USP Webinar on “Overcoming obstacles in establishing pharmacopoeial reference standards: insights from case studies”
- EDQM Training Module 4: Ph. Eur. Reference Standards
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