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

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  • เผยแพร่เมื่อ 10 ก.พ. 2025
  • How to decide impurities in API & Drug Products and their release and shelf life specification

ความคิดเห็น • 21

  • @tamizhselvan655
    @tamizhselvan655 3 ปีที่แล้ว +2

    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.🙂

  • @glorya2908
    @glorya2908 8 หลายเดือนก่อน +2

    Thanks for good information sir

  • @ramanbissa
    @ramanbissa 3 ปีที่แล้ว +2

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

  • @sambhajimasal4248
    @sambhajimasal4248 3 ปีที่แล้ว +1

    SUNDAY morning Motivation 🤩
    Thanks for Your continuous efforts,

  • @khusvikavlogs6958
    @khusvikavlogs6958 ปีที่แล้ว

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

  • @sulakshamunnolli348
    @sulakshamunnolli348 2 ปีที่แล้ว +1

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

  • @vishalanand382
    @vishalanand382 23 วันที่ผ่านมา

    Thankyou so much sir for this information..this helps us a lot ..it will be helpful if you please suggest which software did you use to create this presentation.

  • @ShivamChauhan-xu5cd
    @ShivamChauhan-xu5cd 3 ปีที่แล้ว

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

  • @karnakarkadaru2317
    @karnakarkadaru2317 3 ปีที่แล้ว +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

  • @dhivyasivarajan5393
    @dhivyasivarajan5393 2 ปีที่แล้ว

    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!

  • @neetawagh442
    @neetawagh442 6 หลายเดือนก่อน

    SIR, how to perform dose formation analysis?

  • @rahulkulkarni3037
    @rahulkulkarni3037 3 ปีที่แล้ว +1

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

  • @shantanreddy6487
    @shantanreddy6487 3 ปีที่แล้ว

    Super sir

  • @syedmujeeba884
    @syedmujeeba884 10 หลายเดือนก่อน

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

  • @astaspadiene7346
    @astaspadiene7346 ปีที่แล้ว

    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

  • @durgaprasad-fs2qf
    @durgaprasad-fs2qf 2 ปีที่แล้ว

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

  • @yogeshmandole5953
    @yogeshmandole5953 2 ปีที่แล้ว

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