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Validation of microbiological methods for liquid pharmaceutical forms

  • At: 2006 FIP Congress in Salvadore (Brazil)
  • Type: Poster
  • By: RAMOS, Selma (Lab Farm do Est de Pernambuco, Recife, Brazil)
  • Co-author(s): Reis, Simone (Universidade de Brasília, Brasília, Brazil)
    Alencar, João Rui (Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil)
    Lima, Leduar (Lab Farm do Est de Pernambuco, Recife, Brazil)
    Rolim Neto, Pedro (Universidade Federal de Pernambuco, Recife, Brazil)
  • Abstract:

    Non-sterile products should comply with the pharmacopoeia requirements where the absence of pathogenic microorganisms and viable microorganism count are extolled. The count test is a microbiological method that must be validated by the microorganism recovery parameter (USP 29). Such parameter is constituted in the ability of revering specific

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Last update 4 October 2019

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