FAR || Field Alert Report || USFDA Guideline ||

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  • Опубликовано: 7 сен 2024

Комментарии • 15

  • @dharshanyappo152
    @dharshanyappo152 Год назад +1

    Sir urs explaination is very understanding it will reach all level of person

  • @vps1705
    @vps1705 Год назад +1

    Excellent informative

  • @sanjays1344
    @sanjays1344 2 года назад +2

    Thanks, informative

  • @kausalbhavsar8153
    @kausalbhavsar8153 2 года назад +1

    Fantastic video

  • @manojmodi414
    @manojmodi414 2 года назад +1

    Dear sir,
    Your video is knowledgeable
    Kindly prepare for GLP related videos

  • @ramakrishnaguttula7941
    @ramakrishnaguttula7941 2 года назад +2

    Good video, please post more pharma videos

  • @ramakrishnaguttula7941
    @ramakrishnaguttula7941 2 года назад +2

    Good information

    • @PharmaPill
      @PharmaPill  2 года назад

      Thanks Ramakrishna Garu … :)

  • @manojmodi414
    @manojmodi414 2 года назад +1

    Good morning sir

  • @patilmahavira
    @patilmahavira 2 года назад +1

    Pls tell about process of new and old analytical instrument validation, qualifications and calibration and their flow and procedure

  • @Creativeworld1103
    @Creativeworld1103 Год назад

    Very nicely explained.FAR is for USFDA what about other regulatory .Can you please prepare , how to inform to other regulatory in case of failure.

  • @manojmodi414
    @manojmodi414 2 года назад +1

    Please prepare a video on warning letter

  • @manojmodi414
    @manojmodi414 2 года назад +1

    FEI