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Impurities in medicinal articles are manifold, and of different types. This workshop focuses on elemental impurities (i.e. heavy metals) and describes in a short overview of USP’s approach to the topic with the most relevant general chapters <232> Elemental Impurities- Limits and <233> Elemental Impurities- Procedures.
- Get a regulatory perspective on quality assessment of drug products with respect to DEG/EG as well as elemental impurities.
- Learn about EG-DEG testing in Excipients <469>, <470>.
Why attend
- Learn from leading experts: Gain knowledge from professionals in the field.
- Learn the importance of these tests from a regulatory perspective.
- Network with professionals: Connect with peers from various industries.
- Participate in Q&A sessions: Interact with USP representatives to get your questions answered.
Who should attend
- Quality assurance/quality control specialists
- Regulators & regulatory affairs professionals
- Research and development Scientists
- Contract research organizations
- Contract manufacturing and testing organizations