Enhancing the Quality and Efficiency of Analytical Method Development as Part of the Quality by Design Framework

Highlights of Analytical Chemistry in Switzerland

Authors

  • Christoph Meyer Novartis Pharma AG, PHAD Oral Dosage Forms 2, Forum 1, Novartis Campus, CH-4056 Basel;, Email: christoph.meyer@novartis.com
  • Tomislav Soldo
  • undine Kettenring

DOI:

https://doi.org/10.2533/chimia.2010.825

Keywords:

Analytical method development and validation, Design of experiments(doe), Drug substance (ds) and drug product (dp), Failure mode effects analysis (fmea), Fishbone, Hplc, International committee on harmonization (ich) guidelines, Quality by design (qbd)

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Published

2010-11-26

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