Validation in pharmaceutical industry I Interview Questions and Answers | hindi

Validation in pharmaceutical industry I Interview Questions and Answers | hindi
your quires:
this video based on interview questions and answers for validation department in pharmaceutical industry.
Validation in pharmaceutical industry I Interview questions
Questions covered as follows.
Q.1 : What is validation ?
Q.2 : When we should perform validation ?
Q.3 : What are the major four types of validation ?
Q.4 What is difference between validation and qualification ?
Q.5 : Which guidelines are referred for validation in pharmaceutical industry ?
Q.6 : What are the four types of process validation ?
Q.7 : Why three batches are considered during validation ?
Q.09 : What is validation master plan ?
Q.10 : What is process validation ?
Q.11 : Can we commercialize process validation batches ?
Q.12 : What is revalidation?
Q.13 : What is purpose of cleaning validation ?
Q.14 : What is analytical method validation?
Q.15 : What is validation protocol?
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[@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

[@ranjeetsaini7733]

Nice sir

[@BOL-zo2rw]

Nice brother ❤❤❤❤❤

[@amoltambe6947]

Q7 is GMP guidline

[@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😊

[@debattam2061]

Sir please explain latest process validation guidelines.

[@dhirajk2918]

Turant subscribe kiya sir very good information

[@voiceofkayani5419]

Good

[@pravinsingh8170]

Sir √n+1 expiciant formula kyo lagate hai

[@voiceofkayani5419]

As per GLP & GMP

[@sheetalsharma8986]

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

[@voiceofkayani5419]

@@sheetalsharma8986 ok dear

[@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