How to Decide the Need of Testing Nitrosamine Impurities into Pharmaceuticals?

[@jaiminjani5661]

Excellent deep sharing in short video Thank you sir

[@pradipagarwal2946]

Very informative in a precise manner, appreciate your efforts.

[@ganeshp1938]

With in short period of time given brief information, Great job.

[@dnyansingrajput]

Very deep information in short and smart way you explain such difficult thing... Great sir thank you....

[@pravinbundele3265]

Thanks for excellent presentation and explanation Sir.

[@sambhajimasal4248]

Yes ,so much helpful., Thank you so much,😇 You r my favourite 💥💫

[@narasimhareddy2011]

Very useful information....Thank you.

[@WASIMSHAIKH-cx7dk]

Very informative

[@kishoresarma]

Simple precise information TQ sir

[@G1live]

Hi, Sir. Thanks for providing a worth information. If possible kindly share the presentation.

[@ravindrapandit2993]

Really Useful

[@priyapatel5767]

In case of skip testing & ommision of testing how the risk is assured? Is omission is acceptable?

[@pravinthosare-j4m]

Valuable guidance

[@amsunasara]

What is Acceptance intake limit ?

[@SSK_Yadav]

Very useful

[@deepakpawar1079]

Thank you so much....

[@vivekchoudhary178]

How many batches data is required for establishing the content

[@Learnwithsimon27]

Excellent

[@balajiorchid]

Please do residual solvent video

[@zilurawool8897]

Is it 0.3 ppm or 0.03 ppm

[@mohdazeemuddin8353]

0.03ppm

[@saradaverans]

Thanks sir