Validation in pharmaceutical industry I Interview Questions
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- Опубліковано 10 лип 2024
- Validation in pharmaceutical industry I Interview Questions
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Questions covered
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 : What are stages of process validation ?
Q.8 : What is continued process validation?
Q.9 : Why three batches are considered during validation ?
Q.10 : What is validation master plan ?
Q.11 : What is process validation ?
Q.12 : Can we commercialize process validation batches ?
Q.13 : What is prospective validation ?
Q.14 : What is concurrent validation ?
Q.15 : What is retrospective validation ?
Q.16 : What is revalidation?
Q.17 : What is purpose of cleaning validation ?
Q.18 : What is analytical method validation?
Q.19 : What is validation protocol?
Q.20 : Which department shall prepare validation protocol ?
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Key words:
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Generally, the Quality Department conducts the validation protocol. However, to make it efficient and effective, the Quality Department has to involve QA, QC, and the Quality Engineer (who must have a thorough understanding of the manufacturing process).
This is so helpful, thank you! keep making these kind of videos :)
Thanks
Sir can you make a video about power failure in aseptic pilling process. & Used guide line.
Sure. I will do it
Thank you sir
Quality assurance department
Thanks
can you make videos on decommsioning in pharma imdustry
Thanks for suggesting. I will make soon.
Pls make a video on CIP and SIP , Skid
Ok. I will prepare.
QA department
Thank you sir...
Thanks for reply.
Sir... Can you please make a video about Retention/ control samples... ? Including guidelines
Yes. i will do it
Kindly remove caption,
This is user specific setting. You can do it while whitching videos. Button as 'CC' is there on screen.