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Bio regulatory requirements of pressurized metered dose inhaler (pmdi) and optimizing in- vitro characterization of inhaler

  • At: PSWC, Melbourne (Australia) (2014)
  • Type: Presentation
  • By: AGGARWAL, Deepika (Hyderabad, India)
  • Abstract:

    Background: This covers the current status of regulatory complexity on establishing the bioequivalence of pMDI the limitations of in vitro and in vivo bioequivalence testing, and the practical issues associated with various approaches Objective: Since the in-vitro results are correlating with the in vivo study, before going ahead with the PK and


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Last update 4 October 2019

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