Deviations in Pharmaceutical industry...
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- Опубліковано 7 жов 2024
- In this video, we discussed about the deviation and it's handling procedure, including #initiating, #review, #risk_assessment, #impact_assessment, #investigation, #capa, #approval, #implementation and #closure
#naukri #deviation #pharmaceuticalindustry #qa #qms #qualityassurance #qualitymanagement #qualitymanagementsystem #hindi #interview
Sir you are having good knowledge for learning fresher or experience person
Thanks dear
For knowledge thankyou
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Excellent 👌
❤❤❤❤❤❤
Nice sir bhut badiya mza aa gya
Thanks dear...
Also added....
Additional for CCF .if uh want to revised documents after check the effectiveness of deviation
Nice video sir
Pls give some more information about
SISPQ ND CLOUSER DOCUMENT
Sure...
Good ...Keep Growing 💗
Thanks dear...
Good sir
Thanks dear
Excellent
very helpful 👍
Thanks dear...
Nice sir 👌👌
Thanks dear...
Change control kisme aayega sir
Change Control is a separate QMS tool, and we had discussed change control in another video
ua-cam.com/video/pIsIZzS2NhA/v-deo.html
3 batch banane hoga to kya strength same hoga
When we say 3batches of same product, it means same batch size, same strength
Qms pe video banaiye
We have a separate video on QMS
ua-cam.com/video/wrDGM9YPFGw/v-deo.html
Do not use example from outside from pharmaceutical industries e. g vimbar example. Give real example
Sure... you will find the same in near future but in this video I had made the attempt to make them understand in a more familiar way, so given that example...
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