How to decide impurities in API & Drug Products and their release and shelf life specification
Пікірлер: 20
@glorya29082 ай бұрын
Thanks for good information sir
@khusvikavlogs69589 ай бұрын
Great work sir i get lot of motivation and knowledge from your videos
@tamizhselvan6552 жыл бұрын
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.🙂
@ramanbissa2 жыл бұрын
very nice effort, it is the first channel of it's kind...
@pharmagrowthhub30832 жыл бұрын
Thanks a lot 😊
@sambhajimasal42482 жыл бұрын
SUNDAY morning Motivation 🤩 Thanks for Your continuous efforts,
@sulakshamunnolli3482 жыл бұрын
Perfect lecture ....thanks Bhaskar...hope you are doing great
@karnakarkadaru23172 жыл бұрын
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
@ShivamChauhan-xu5cd2 жыл бұрын
Learning is a treasure that will follow its owner everywhere... Thanks a lot... (How can I connect with you? Kindly share details )
@astaspadiene7346 Жыл бұрын
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
@pharmagrowthhub3083 Жыл бұрын
Sure, Asta!
@syedmujeeba8845 ай бұрын
dear sir, Please explain on refernce stnadrds, primary standard , working standard, compendial standards
@dhivyasivarajan53932 жыл бұрын
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!
@neetawagh44222 күн бұрын
SIR, how to perform dose formation analysis?
@rahulkulkarni30372 жыл бұрын
Where can we get registered specification of impurities ANDA or NDA?
@shantanreddy64872 жыл бұрын
Super sir
@yogeshmandole5953 Жыл бұрын
On what basis you decide to qualify 1.5% for shelf life limit, why not 2%
@durgaprasad-fs2qf Жыл бұрын
Dear sir, pls refer me where I have to find out the information about all known impurities limits,TD50,LD50 values ?