Good Automated Manufacturing Practice GAMP 5

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  • Опубликовано: 24 окт 2024

Комментарии • 12

  • @jagadeeshponnada8628
    @jagadeeshponnada8628 4 месяца назад

    Thank you sir

  • @shanhoney1538
    @shanhoney1538 2 года назад +2

    Sir, thank you for valuable information about GAMP. Please explain about risk management along with FMEA along with example sheet.

  • @ranapratapnaidu
    @ranapratapnaidu 9 месяцев назад

    Dear sir,please share the full videos on csv..

  • @yoganandish84
    @yoganandish84 2 года назад +2

    The critical activities involved in concept phase was missed out in presentation 1. Software and hardware Category 2. GxP impact assessment 3. ER&ES assessment should be performed in concept phase.

  • @ashokashok-te3ky
    @ashokashok-te3ky Год назад

    Sir computer system validation includes all the tools, what are the tools that are useful for us in the main

  • @tb279677
    @tb279677 11 месяцев назад

    Are there any videos like this where the presenter speaks English as their first language??

  • @braedonmendez5931
    @braedonmendez5931 2 года назад

    Has anyone performed a GAP assessment on TrackLink?

  • @mdimranhossain9495
    @mdimranhossain9495 Год назад

    Sir how to download ispe guideline freely? Have any scope

  • @ashwinirenikindi
    @ashwinirenikindi 2 года назад

    How do we create protocols ?

  • @veereshhiremath8666
    @veereshhiremath8666 2 года назад

    Is coding required in life science csv

    • @lifesciencecareerlearning7180
      @lifesciencecareerlearning7180  2 года назад

      No veeresh, coding is not required for csv role in pharmaceutical. Most of the time you will do qualifications, protocol creation and review.