Thanks for good information sir

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

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.🙂

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

SUNDAY morning Motivation 🤩 Thanks for Your continuous efforts,

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

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

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

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

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

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!

SIR, how to perform dose formation analysis?

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

Super sir

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

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