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Determination of digoxin residues on manufacturing equipment surfaces in cleaning validation process

  • At: 2008 FIP Congress in Basel (Switzerland)
  • Type: Poster
  • By: OMEROVIC, Samira (Bosnalijek, Pharmaceutical and Chemical Industry, Sarajevo, Bosnia and Herzegovina)
  • Co-author(s): Dizdarevic, Aida (Bosnalijek, Pharmaceutical and Chemical Industry, SARAJEVO, Bosnia and Herzegovina)
    Buturovic, Mihneta (Bosnalijek, Pharmaceutical and Chemical Industry, SARAJEVO, Bosnia and Herzegovina)
  • Abstract:

    cGMP, FDA and ICH regulations have resulted in cleaning validation becoming an essential part of the production of drugs and active pharmaceutical ingredients. In many cases, the same equipment may be used for processing different products. To avoid contamination of the following product, adequate cleaning procedures are essential.

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Last update 4 October 2019

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