Deviations in Pharmaceutical industry l Interview Questions answers | Hindi
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- Опубліковано 8 лют 2024
- Deviations in Pharmaceutical industry l Interview Questions answers | Hindi
your quires;
This video based on interview questions and answers regarding Daviation in pharmaceutical industry.
Here are the selected top interview questions about deviations in pharmaceutical industry
Questions covered:
Q.1 :What is Deviation?
Q.2: Why we should raise deviation?
Q.3: What is difference between incident and deviation?
Q.4: What are the categories / classifications of deviation?
Q.5: What is thumb rule for writing deviation description?
Q.6: Planned deviations shall be raised or not ?
Q.7: What are the three stages / Levels of deviation?
Q 8: Why review of previous deviations is done during investigation ?
Q.9: Why we should raise deviation within 24 hours of identification?
Q.10: What are the trigger points for deviation?
Q.11: Which guideline most commonly referred for deviation handling ?
Q.12: Why deviation count is important in QMS ?
Q.13: Can we re-open closed deviation ?
Q.14: Whether we should raise deviation for OOS / OOT results ?
Q.15: Can we cancel close raised deviation ?
Q.16: Can we cover / address multiple discrepancies in single deviation ?
Q.17: What are the most common root causes for deviations?
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Key words:
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Thanks for sharing information
Just keep watching and sharing
Very good information thanks
Thank you sir ❤
❤
Sir aap ek vedeo reviewer and Astt. Manager pr bhi banaye.
Ok dear
Sir ap qms pe video banaiye
Sure
Which is guidline of deviation
ICH guidelines used.
ICH Q-10
Guidelines ?
For Daviation.
Check ich guidelines,
Sir deviation kitne type ke hote hai palned nad non planned
Daviation classified in 3 types.
1 minor Daviation
2 major Daviation
3 critical Daviation and
Also decided into
Plan Daviation and
UN plan Daviation
Sir planned deviation now change in temporary change control????
@jeetbrothers9590 have to see the guidelines for update