Maximising HPLC Productivity

18 - 20 April 2012
Conference
Prague, Czech Republic

The purpose of this course is to provide attendees with practical information to manage HPLC within GMP-/FDA-regulated environments of the pharmaceutical industry by combining science and compliance. The emphasis will be on the following science and compliance issues:

  • Miniaturisation of HPLC: advantages and disadvantages
  • Sampling practices and pitfalls
  • Sample preparation for HPLC
  • Latest enforcement issues and lessons for CDS
  • Science driven HPLC qualification
  • Method development and validation including understanding and trouble shooting problems
  • USP and EP system suitability tests
  • Practical chromatographic integration
  • Better working to avoid OOS investigations
  • Generating productivity gains through the validation of a CDS
  • Defining and protecting CDS electronic records
  • Documentation for HPLC

Organiser: Concept Heidelberg

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