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Establishment of new dissolution specification in monographs of the Korean Pharmacopoeia: Tiaprofenic acid tablets and Tinidazole tablets

  • At: 2017 FIP Congress in Stockholm (Sweden)
  • Type: Poster
  • By: CHUN, In Koo (Dongduk Women's University / The Society of Korean Official Compendium for Public Health, College of Pharmacy / Official compendia Research, Seoul, Korea, Republic Of)
  • Co-author(s): In Koo Chun: The Society of Korean Official Compendium for Public Health, Seoul, Korea, Republic Of;College of Pharmacy, Dongduk Women’s University, Seoul, Korea, Republic Of
    Kwan Hyung Cho: College of Pharmacy, Inje University, Gimhae, Korea, Republic Of
    Dong-Jin Jang: Department of Pharmaceutical Engineering, Inje University, Gimhae, Korea, Republic Of
    Dae Hun Kim: Collage of Pharmacy, Inje University, Gimhae, Korea, Republic Of
  • Abstract:

    Backgrounds

    Dissolution is a good property to prevent marked biononequivalence of oral solid dosage forms, and to assure the quality consistency of drug product through its life-cycle. Therefore, by referring to ICH Q6A, setting dissolution acceptance criterion is required for the compendial monographs having disintegration test alone. 

    Aims

    Purpose

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Last update 4 October 2019

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