Validation in pharmaceutical industry I Interview Questions and Answers | hindi

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  • Опубликовано: 21 окт 2024

Комментарии • 27

  • @ALPSPHONE
    @ALPSPHONE 7 месяцев назад +2

    Sir very easy or simple way explained for understanding any person

  • @ChessTackling
    @ChessTackling 7 дней назад +1

    Superb😊

  • @ashoksarkar7951
    @ashoksarkar7951 2 месяца назад +2

    Thank you sir one question plesae hold time analysis ka total duration time sample kitna din tak rakh sakte hai

    • @voiceofkayani5419
      @voiceofkayani5419  2 месяца назад

      Will make video on this topic in details...
      Keep watching

  • @ranjeetsaini7733
    @ranjeetsaini7733 6 месяцев назад +2

    Nice sir

  • @amoltambe6947
    @amoltambe6947 2 месяца назад +2

    Q7 is GMP guidline

  • @BOL-zo2rw
    @BOL-zo2rw Месяц назад +3

    Nice brother ❤❤❤❤❤

  • @monicakhetan415
    @monicakhetan415 2 месяца назад +2

    Dear Sir, during 3 consecutive batches if 2nd batch gets OOS or dev..then what shld b done

    • @voiceofkayani5419
      @voiceofkayani5419  2 месяца назад

      @@monicakhetan415 repeat process

    • @monicakhetan415
      @monicakhetan415 2 месяца назад +2

      It means v shld take another 3 batches?? N also what can be done with that oos batch

    • @voiceofkayani5419
      @voiceofkayani5419  2 месяца назад

      @@monicakhetan415 yes if one batch in 3 consecutive batch failed.
      Process will be repeated for one failed batch
      Not be considered. It depends also that what is the stage of process and it depends on your company culture...
      2 batches will be considered
      1 batch will be repeated..

    • @monicakhetan415
      @monicakhetan415 2 месяца назад +1

      Thank you so much sir😊

  • @debattam2061
    @debattam2061 6 месяцев назад

    Sir please explain latest process validation guidelines.

  • @dhirajk2918
    @dhirajk2918 5 месяцев назад +1

    Turant subscribe kiya sir very good information

  • @pravinsingh8170
    @pravinsingh8170 7 месяцев назад +3

    Sir √n+1 expiciant formula kyo lagate hai

  • @pravinsingh8170
    @pravinsingh8170 7 месяцев назад +1

    Agar protocol me kon kon sa paramter hote hai

    • @voiceofkayani5419
      @voiceofkayani5419  7 месяцев назад

      Validation ka protocol Mai validation k parameters hongai

  • @sheetalsharma8986
    @sheetalsharma8986 2 месяца назад +2

    Next time please add subtitles, it’s very hard to understand your accent .

  • @pravinsingh8170
    @pravinsingh8170 6 месяцев назад +1

    Sir ek question hai agar frability fail ho rahi 1persanatge se jaida ho raha to phir guideline kya kahta hai repat test kare

    • @voiceofkayani5419
      @voiceofkayani5419  6 месяцев назад +1

      If friability fails in first attempt. Then repeat the test twice in same manner and the average results of 3 values should be less than 1%

  • @Easy_Art_2024
    @Easy_Art_2024 3 месяца назад +1

    Q7 , method validation ki guidelines nhi hai, ap galat info de rhe h

    • @voiceofkayani5419
      @voiceofkayani5419  3 месяца назад +1

      Dear,
      Video ko sokoon se daikhain phir baat kariya tasalli se....me ne kahin nai kaha k Q7 specifically used for method Validation.,
      Q7 support karta hai best validation k process ko., method Validation ka Naam nai hai video Mai...
      Q7 guidelines k 7 sections Hain jinka purpose best PRODUCTION produce Karna hai and Q7 support process validation..or process Validation hoga to ap good manufacturing kar Sakai gai...
      Thanks for your concerns

  • @pravinsingh8170
    @pravinsingh8170 7 месяцев назад +1

    Sampling me