How to decide impurities in API & Drug Products and their release and shelf life specification

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  • čas přidán 26. 11. 2021
  • How to decide impurities in API & Drug Products and their release and shelf life specification
  • Věda a technologie

Komentáře • 20

  • @glorya2908
    @glorya2908 Před měsícem +2

    Thanks for good information sir

  • @khusvikavlogs6958
    @khusvikavlogs6958 Před 9 měsíci

    Great work sir i get lot of motivation and knowledge from your videos

  • @tamizhselvan655
    @tamizhselvan655 Před 2 lety +1

    Hello sir. I am working in analytical research and development your videos are very useful for me thank you and keep continuing your effort sir...I am come to lot of this after seeing your videos.🙂

  • @sambhajimasal4248
    @sambhajimasal4248 Před 2 lety +1

    SUNDAY morning Motivation 🤩
    Thanks for Your continuous efforts,

  • @ramanbissa
    @ramanbissa Před 2 lety +2

    very nice effort, it is the first channel of it's kind...

  • @sulakshamunnolli348
    @sulakshamunnolli348 Před 2 lety +1

    Perfect lecture ....thanks Bhaskar...hope you are doing great

  • @shantanreddy6487
    @shantanreddy6487 Před 2 lety

    Super sir

  • @neetawagh442
    @neetawagh442 Před 5 dny

    SIR, how to perform dose formation analysis?

  • @karnakarkadaru2317
    @karnakarkadaru2317 Před 2 lety +1

    Hi sir, I could not get clarity on this topic. If we have to qulifiy Impurity
    specification rather than release specification. What is the criteria as per guidline and how much level of imp is safety. What are the doccument should be generate to getting the self-life specification. Please make a video by elaborating the topic.
    Thanking you sir

  • @syedmujeeba884
    @syedmujeeba884 Před 4 měsíci

    dear sir, Please explain on refernce stnadrds, primary standard , working standard, compendial standards

  • @ShivamChauhan-xu5cd
    @ShivamChauhan-xu5cd Před 2 lety

    Learning is a treasure that will follow its owner everywhere... Thanks a lot... (How can I connect with you? Kindly share details )

  • @rahulkulkarni3037
    @rahulkulkarni3037 Před 2 lety +1

    Where can we get registered specification of impurities ANDA or NDA?

  • @dhivyasivarajan5393
    @dhivyasivarajan5393 Před 2 lety

    Hi,
    Your videos are very helpful and easy to understand. Only request/suggestion would be order the video content as it would make the viewers to have a flow in the content.
    Great job and thanks for the effort!

  • @durgaprasad-fs2qf
    @durgaprasad-fs2qf Před rokem

    Dear sir, pls refer me where I have to find out the information about all known impurities limits,TD50,LD50 values ?

  • @astaspadiene7346
    @astaspadiene7346 Před 11 měsíci

    Hello,
    I am writing to you from the Lithuania University of Health Science. I would like to ask your permission to use this video in my lecture and show it to my students. The video will be shown for educational purposes only.
    I look forward to hearing from you and hope you will agree to share your presentation.
    Kind Regards,
    Asta Špadienė

  • @yogeshmandole5953
    @yogeshmandole5953 Před rokem

    On what basis you decide to qualify 1.5% for shelf life limit, why not 2%