Deviations in Pharmaceutical industry l Interview Questions answers | Hindi

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:
deviations in pharmaceutical industry
data integrity in pharmaceutical industry
pharmaceutical industry
capa in pharmaceutical industry
change control in pharmaceutical industry
deviation classification
pharmaceutical
environmental controls
mechanical failure
sampling of incoming materials
deviations
industry
deviation
quality management system
process control parameters
line clearance
critical deviation
how to handle
mixed lots on pallets
examples of deviation
voice of kayani
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[@mogheezahmed7735]

Amzing

[@pravinsingh8170]

Sir ap qms pe video banaiye

[@voiceofkayani5419]

Sure

[@akhileshpandey4491]

Very good information thanks

[@rajankalia681]

Sir sample procedure par video bna dijiye sample in granulation compression of validation batch

[@javednalband6155]

Thank you sir ❤

[@LAKHANSINGH-ju9jx]

Thanks for sharing information

[@voiceofkayani5419]

Just keep watching and sharing

[@DaviationPlanes]

For the creator of this: #daviation is made for my channel. Just so you know, it isn’t anything associated with deviation. You can keep it like this and I’m not hating or something

[@itzkalaakaar1015]

Sir OOS and OOT ke lie konsi guideline hai?

[@itzkalaakaar1015]

Kitne time period mai OOS activity complete karni chahie?

[@voiceofkayani5419]

You can check ICH GUIDELINES

[@voiceofkayani5419]

Not so specific time....
Depends on case ,, normally within 2 to 3 days or in 1 day .....
It depends on situation but need to complete as soon as possible

[@NaveenKumar-xu2hu]

Sir aap ek vedeo reviewer and Astt. Manager pr bhi banaye.

[@voiceofkayani5419]

Ok dear

[@pravinsingh8170]

Sir deviation kitne type ke hote hai palned nad non planned

[@voiceofkayani5419]

Daviation classified in 3 types.
1 minor Daviation
2 major Daviation
3 critical Daviation and
Also decided into
Plan Daviation and
UN plan Daviation

[@jeetbrothers9590]

Sir planned deviation now change in temporary change control????

[@voiceofkayani5419]

@jeetbrothers9590 have to see the guidelines for update

[@neyazahmad1787]

❤

[@pawanpatel8980]

Deviation ki gideline kya hi

[@voiceofkayani5419]

FDA 21, CFR PART 211.160 and
FDA 21 CFR PART 211.192

[@muhammadzohaib7640]

Guidelines ?

[@voiceofkayani5419]

For Daviation.
Check ich guidelines,

[@santoshkhilari2090]

Which is guidline of deviation

[@voiceofkayani5419]

ICH guidelines used.
ICH Q-10