U.S. FDA eCTD Requirements for Drug Master Files (DMFs)

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  • Опубликовано: 29 дек 2024

Комментарии • 4

  • @varshareddy-we3dv
    @varshareddy-we3dv Год назад

    Hi ..why we need to submit DMF ,where as we already submitting the API snd mfg.data in dossier eCTD .please tell d rational behind that

  • @manalsaleh5100
    @manalsaleh5100 4 года назад +1

    Can I have pdf of this material?

  • @cartoondrug9989
    @cartoondrug9989 8 месяцев назад

    Hello mam can you plz provide me any ctd dossier file sample

  • @kavyanainita9873
    @kavyanainita9873 4 года назад

    Where can I find eCTD submission requirements for USA