Toxic Impurities in Active Pharmaceutical Ingredients

Toxic Impurities in Active Pharmaceutical Ingredients is a webinar that covers topics such as:

  • Handling trace analysis
  • General Information about the limits for toxic impurities
  • Structure and properties of NDEA
  • Structure and properties of NDMA
  • How are nitrosamines formed?
  • Structure and properties of NMBA
  • Some thoughts on other potential toxic impurities
  • How did it get in sartans?

Toxic Impurities in Active Pharmaceutical Ingredients is intended for:

  • Research and Development Departments
  • Quality Departments
  • Validation Departments
  • Regulatory Affairs Departments
  • Everyone involved with New Product Selection
  • Everyone involved with Analytical Method Development and Validation

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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