Sterile Injectable Manufacturing Process ( Part 2)

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  • Опубликовано: 2 окт 2024

Комментарии • 8

  • @achyutjagdhane9683
    @achyutjagdhane9683 2 года назад +1

    dear palash , very good clarity on subject , good luck for your journey

  • @mdimranhossain9495
    @mdimranhossain9495 5 месяцев назад +1

    Sir, will you please answer my below question.
    Why ampoule products require sterilization and vial products for depyrogenation.
    Can we use depyrogenation tunnel for ampoule product

    • @cGMP
      @cGMP  4 месяца назад

      Yes, depyrogenation tunnel can be used for Vial and Ampoule both in case of aseptic manufacturing process.

    • @mdimranhossain9495
      @mdimranhossain9495 4 месяца назад

      @@cGMP what is the differences between aseptic & sterile process.

  • @jirensama1622
    @jirensama1622 2 года назад

    I just wanted to know -
    Filteration of the Drug product which is in the holding vessel is happening in the Grade C area with Laminar air flow Grade A? - Terminal sterilization
    And filteration and sterilization of Drug product which is in the holding vessel is happening in the Grade B area with Grade A laminar air flow - Asceptic sterilization
    Is this correct?

    • @cGMP
      @cGMP  2 года назад

      Yes, Grade C under laminar air flow is appropriate for product produce in Terminal Sterilisation facility

  • @jirensama1622
    @jirensama1622 2 года назад +1

    Also in the previous video you mentioned that cleaning of primary packaging materials such as vials is happened in the grade D area whereas now you're saying it's happening in the Grade C area?
    Can you confirm where it happens?

    • @cGMP
      @cGMP  2 года назад

      Grade C area will be appropriate for Vial washing.