Validation in pharmaceutical industry I Interview Questions and Answers

Validation in pharmaceutical industry I Interview Questions and Answers | hindi

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Күн бұрын

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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Пікірлер: 25

@amoltambe6947 15 күн бұрын

Q7 is GMP guidline

@user-hi1ni8qg1y 5 ай бұрын

Sir very easy or simple way explained for understanding any person

@voiceofkayani5419 5 ай бұрын

Just keep watching and sharing

@ashoksarkar7951 11 күн бұрын

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

@voiceofkayani5419 11 күн бұрын

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

@ranjeetsaini7733 4 ай бұрын

Nice sir

@dhirajk2918 3 ай бұрын

Turant subscribe kiya sir very good information

@voiceofkayani5419 3 ай бұрын

Good

@debattam2061 4 ай бұрын

Sir please explain latest process validation guidelines.

@pravinsingh8170 5 ай бұрын

Sir √n+1 expiciant formula kyo lagate hai

@voiceofkayani5419 5 ай бұрын

As per GLP & GMP

@sheetalsharma8986 26 күн бұрын

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

@voiceofkayani5419 26 күн бұрын

@@sheetalsharma8986 ok dear

@Easy_Art_2024 Ай бұрын

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

@voiceofkayani5419 Ай бұрын

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

@monicakhetan415 Күн бұрын

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

@voiceofkayani5419 Күн бұрын

@@monicakhetan415 repeat process

@monicakhetan415 Күн бұрын

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

@voiceofkayani5419 Күн бұрын

@@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 20 сағат бұрын

Thank you so much sir😊

@pravinsingh8170 5 ай бұрын

Agar protocol me kon kon sa paramter hote hai

@voiceofkayani5419 5 ай бұрын

Validation ka protocol Mai validation k parameters hongai

@pravinsingh8170 4 ай бұрын

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

@voiceofkayani5419 4 ай бұрын

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 5 ай бұрын

Sampling me