Validation in pharmaceutical industry I Interview Questions and Answers | hindi

[@ALPSPHONE]

Sir very easy or simple way explained for understanding any person

[@voiceofkayani5419]

Just keep watching and sharing

[@ashoksarkar7951]

Thank you sir one question plesae hold time analysis ka total duration time sample kitna din tak rakh sakte hai

[@voiceofkayani5419]

Will make video on this topic in details... Keep watching

[@amoltambe6947]

Q7 is GMP guidline

[@BOL-zo2rw]

Nice brother ❤❤❤❤❤

[@monicakhetan415]

Dear Sir, during 3 consecutive batches if 2nd batch gets OOS or dev..then what shld b done

[@voiceofkayani5419]

@@monicakhetan415 repeat process

[@monicakhetan415]

It means v shld take another 3 batches?? N also what can be done with that oos batch

[@voiceofkayani5419]

@@monicakhetan415 yes if one batch in 3 consecutive batch failed. Process will be repeated for one failed batch Not be considered. It depends also that what is the stage of process and it depends on your company culture... 2 batches will be considered 1 batch will be repeated..

[@monicakhetan415]

Thank you so much sir😊

[@sheetalsharma8986]

Next time please add subtitles, it’s very hard to understand your accent .

[@voiceofkayani5419]

@@sheetalsharma8986 ok dear

[@debattam2061]

Sir please explain latest process validation guidelines.

[@pravinsingh8170]

Sir √n+1 expiciant formula kyo lagate hai

[@voiceofkayani5419]

As per GLP & GMP

[@ranjeetsaini7733]

Nice sir

[@dhirajk2918]

Turant subscribe kiya sir very good information

[@voiceofkayani5419]

Good

[@pravinsingh8170]

Agar protocol me kon kon sa paramter hote hai

[@voiceofkayani5419]

Validation ka protocol Mai validation k parameters hongai

[@Easy_Art_2024]

Q7 , method validation ki guidelines nhi hai, ap galat info de rhe h

[@voiceofkayani5419]

Dear, Video ko sokoon se daikhain phir baat kariya tasalli se....me ne kahin nai kaha k Q7 specifically used for method Validation., Q7 support karta hai best validation k process ko., method Validation ka Naam nai hai video Mai... Q7 guidelines k 7 sections Hain jinka purpose best PRODUCTION produce Karna hai and Q7 support process validation..or process Validation hoga to ap good manufacturing kar Sakai gai... Thanks for your concerns

[@pravinsingh8170]

Sir ek question hai agar frability fail ho rahi 1persanatge se jaida ho raha to phir guideline kya kahta hai repat test kare

[@voiceofkayani5419]

If friability fails in first attempt. Then repeat the test twice in same manner and the average results of 3 values should be less than 1%

[@pravinsingh8170]

Sampling me