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Why Non Viable Particle Count Required when We are Doing Viable Count? ‪@PHARMAVEN‬ #validation
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7 Views • Aug 18, 2024 • Click to toggle off description
What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality ‎@PHARMAVEN  #gmp

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How to Face USFDA Audits GMP

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USFDA How To Behave in Audit Room While Facing Regulatory Inspection


GMP, How To Behave in Audit Room, Facing Regulatory Inspection part 5 #audits #success #PHARMA #GMP

This video is about acceptable behaviour patterns in an audit room, talks about clothing, personal behaviour, do's and don'ts and How to help others during an audit.

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Part 2 of series About How to Face Regulatory Inspection, this part focused on How to answer questions in regulatory inspection

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Few Insights on How to be Successful in Regulatory Inspection in Pharmaceutical Industry, Mainly on Personnel Practices and Procedures

GMP, How to Face Audits, #pharma #Regulations #audits #success #GMP #PHARMA

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How to face USFDA Audit
How to face Audit
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How to behave in audit Room
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Dhaval Surti

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Few Insights on How to be Successful in Regulatory Inspection in Pharmaceutical Industry, Mainly on Personnel Practices and Procedures

Few Insights on How to be Successful in Regulatory Inspection in Pharmaceutical Industry, Mainly on Personnel Practices and P
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Uploaded At Aug 18, 2024 ^^


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RYD date created : 2024-08-18T20:06:12.93978Z
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6 Comments

Top Comments of this video!! :3

@vlog-ed3ul

2 months ago

Question bhi kafi achha tha aur jabab bhi thank both of you

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@CAToons19

3 months ago

Sir Thank you very much for reaching my question clearing my doubt
Thankyou you sir thank you very much

1 |

@factxman9865

3 months ago

Sir ek media filling ke upar proper video

3 |

@vlog-ed3ul

2 months ago

सर मेरा एक सवाल है
Non- viable particle count करते समय 0.5 और 5.0 के size के ही particle क्यु count किए जाते हैं जबकि एरिया में और भी sizes के पार्टिकल मौजूद होते हैं जो प्रोडक्ट मे contamination कर सकते हैं

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