Equipment Validation I Pharmaceutical Industry l DQ IQ IQ PQ

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  • เผยแพร่เมื่อ 24 ม.ค. 2025

ความคิดเห็น •

  • @5669262309
    @5669262309 ปีที่แล้ว +2

    Thank you madam. And ur explanation is very simply understand anyone. Thank you.
    Plz send that link about remaining validations.

    • @simplifypharma
      @simplifypharma  ปีที่แล้ว +1

      I will upload those videos asap

    • @simplifypharma
      @simplifypharma  ปีที่แล้ว +1

      Kindly refer the channel for more validation videos

  • @ashishgajjar7056
    @ashishgajjar7056 5 หลายเดือนก่อน +1

    Very useful video, easy to learn method with easy examples.
    Nice ma'am 🎉

  • @PHARMAACQUAINTANCE
    @PHARMAACQUAINTANCE 4 หลายเดือนก่อน +1

    Wow very helping video 😊😊😊

  • @abdullahalasri6682
    @abdullahalasri6682 2 ปีที่แล้ว +1

    Thank you for the effort and clear well explained presentation

    • @simplifypharma
      @simplifypharma  ปีที่แล้ว

      Your comments are what keep me motivated

  • @TheNyakaat
    @TheNyakaat 3 หลายเดือนก่อน +1

    Very clear explanation!

  • @RAJATSAYYED
    @RAJATSAYYED 2 ปีที่แล้ว +1

    Very nicely explained

  • @playlistajsy4486
    @playlistajsy4486 ปีที่แล้ว +2

    Will you please elaborate each phase of equipment qualification with listed
    (1) how design protocol, what is the basic approach and require thing to design protocol, reference of protocol design
    (2) any common considerations in protocol design irrespective of equipment make mechanism function etc. Eg. Safety, risk assessment, challenge studies, product runs like that are any more.
    (3) what we have to do if we observed non intrensic failures of equipment qualification
    (4) how to schedule calibration, preventive maintenance
    (5) how we can recommend preventive maintenance, in what way, what we need, and references of preventive maintenance etc etc

  • @argentosebastian
    @argentosebastian 10 หลายเดือนก่อน

    What gmp stand for?

    • @simplifypharma
      @simplifypharma  10 หลายเดือนก่อน

      Good Manufacturing Practices