He is the best teacher I have seen in youtube , it was difficult to understand this analytical method validation I repeated many times now I get the right teach

Bhaskar sir very good topic you have discussed very precisely.

Thank you sir for your very clear concept. I have gone through several tutorials of Analytical Method Validation for getting a clear concept. Finally I have got the desired one, which I have been looking for a long since. Thank you Again 💙

thanks sir for your valuable guidance , very few peoples in pharma industry gives such a guidance , thanks a lot

It’s very helpful 😊

Excellent video sir 👏👏👏

Dear Bhaskar, thank you so mucj for this video. It was explained in full details and it helped me a lot with the studying material I'm dealing atm. Maybe it would be a good idea to put the name of the methods somewhere in the corner of the video so when we skip the video forward or back (depending on what we need) to find it more easily. Thank you once again! 😊

This was a great review for me as I am currently job searching after a 5 month break. Thank you.

Very well explained...thank you sir

You have the best knowledge on what your teaching boss

Very knowldegabke explanation Sir, Thank you. Like to join and learn from Pharma Hub soon. At 20:00 while narrowing the range of pH you bymistakely increased the range from 4.2.

Thanku so much sir for providing a great knowledge of AMV

Great content

Thank you sir... given useful information

Great work sir....

Sir, could u please,explain how to set peak purity parameter in agilent

Thank you very much for your videos ☺️☺️☺️ sir

Thank you sir,...

Quality

Thank you very much Sir

Too good

Pls keep a session on GC method development

Thank you so much sir 🙏🤩😍

Thanks a lot sir

Give recovery calculations with example

Specificity selectivity same or different

Thanks sir

👏👏👏👏👏👏👏thank you

In specificity parameter, when impurities are unavailable, ICH guideline said to use a second well characterized producer e.g. pharmacopeial method or other validation method. Can you please explain, when we have an other second well characterized method, than why we are doing this validation exercise on new one?

Hi Yogesh here

Sir from where we take the acceptance criteria for the parameters?

If 150mg/day MDD then what is impurities limit.

Tq sir

Why accuracy performed in 3set sir?

Sir why 6 sets are choosen for reproducibility..??

Thank you Sir