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

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

[@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.

[@deepakpawar1079]

Thank you so much....

[@narasimhareddy2011]

Very useful information....Thank you.

[@sambhajimasal4248]

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

[@ravindrapandit2993]

Really Useful

[@user-oz6yk6mg7u]

Valuable guidance

[@kishoresarma]

Simple precise information TQ sir

[@Learnwithsimon27]

Excellent

[@G1live]

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

[@SSK_Yadav]

Very useful

[@saradaverans]

Thanks sir

[@priyapatel5767]

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

[@balajiorchid]

Please do residual solvent video

[@amsunasara]

What is Acceptance intake limit ?

[@vivekchoudhary178]

How many batches data is required for establishing the content

[@zilurawool8897]

Is it 0.3 ppm or 0.03 ppm

[@mohdazeemuddin8353]

0.03ppm