हिन्दी में पार्ट 2, Media Fill Failure Investigation

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  • Опубликовано: 12 сен 2024

Комментарии • 17

  • @PHARMAVEN
    @PHARMAVEN  2 года назад +1

    हिन्दी में, Media Fill Failure Investigation in Hindi @PharMaven #media #aseptic #pharma #usfda

  • @durgareddy3908
    @durgareddy3908 2 года назад +2

    Thanks for information 👍👍👍

  • @vipulchavda9583
    @vipulchavda9583 2 года назад +1

    Sir ase hi hindi me our video banate rahe hame parfect samaj me aata he

  • @expofield3004
    @expofield3004 Год назад +1

    Nice video and content

  • @drmustinlogen9027
    @drmustinlogen9027 8 месяцев назад +1

    Very nice

  • @Rahulsingh-mz7qv
    @Rahulsingh-mz7qv Месяц назад +1

    Very nice sir

  • @deepaksukaralia577
    @deepaksukaralia577 2 года назад +1

    Well explained sir 👏 👌

  • @rajarao6563
    @rajarao6563 2 года назад +1

    Superb sir ji

  • @nirmalsartana4061
    @nirmalsartana4061 2 года назад +1

    Well explained sir

  • @bharatsinh7275
    @bharatsinh7275 2 года назад +1

    Good Information

    • @PHARMAVEN
      @PHARMAVEN  2 года назад

      Thanks, please also share to more friends

  • @sanjaypatel2025
    @sanjaypatel2025 Год назад +1

    sir Ek video microbial limit test or Raw materials and finish product bano🙏

  • @vishalmangukiya5844
    @vishalmangukiya5844 Год назад +1

    Sir Please make video on Container closure integrity.

  • @sanjaypatel2025
    @sanjaypatel2025 Год назад +1

    sir hama personnel monitoring ke video chiya

  • @krishnadesai6953
    @krishnadesai6953 Год назад +1

    Ccit...when require

  • @jyotirmayapanda7193
    @jyotirmayapanda7193 Год назад +1

    What may be the reason initial and end stage media fill vials pass but middle stage failed ?

    • @PHARMAVEN
      @PHARMAVEN  Год назад

      Many reasons
      1. Any intervention which was not executed properly
      2. New intervention
      3. Air flow not maintained
      4. Opening filling machine door
      5. Differential pressure low
      6. One of component, such as rubber stoppers or vials not properly sterilized
      7. New operator introduced without proper aseptic Processing training
      8. NVPC count increased
      9. Any component such as filling needle, syringe, tubing or connection changed