Equipment Validation I Pharmaceutical Industry l DQ IQ IQ PQ

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  • Опубліковано 22 жов 2024

КОМЕНТАРІ • 16

  • @5669262309
    @5669262309 Рік тому +2

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

  • @PHARMAACQUAINTANCE
    @PHARMAACQUAINTANCE Місяць тому +1

    Wow very helping video 😊😊😊

  • @ashishgajjar7056
    @ashishgajjar7056 2 місяці тому +1

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

  • @abdullahalasri6682
    @abdullahalasri6682 Рік тому +1

    Thank you for the effort and clear well explained presentation

  • @playlistajsy4486
    @playlistajsy4486 Рік тому +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

  • @RAJATSAYYED
    @RAJATSAYYED 2 роки тому +1

    Very nicely explained

  • @argentosebastian
    @argentosebastian 7 місяців тому

    What gmp stand for?