Environmental monitoring (EM) in pharmaceutical industry I 16 Interview questions and answers

Environmental monitoring (EM) in pharmaceutical industry I 16 Interview questions and answers
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Go to below playlists and search for a topic you want:

1. QMS - Quality Management System in Pharmaceutical industry :    • QMS - Quality Management System in Ph...  
2. QA- Quality assurance in Pharmaceutical industry. :    • QA- Quality assurance in Pharmaceutic...  
3. QC - Quality Control in Pharmaceutical industry :    • QC - Quality Control in Pharmaceutica...  
4. OSD - Tablet Manufacturing in Pharmaceutical industry :    • OSD - Tablet Manufacturing in Pharmac...  
5. Injectable processing - Injectable processing or Sterile dosage formulation :    • Injectable processing - Injectable pr...  

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Questions covered:
Q. What is environmental monitoring (EM) in the pharmaceutical industry?
Q. What are the key components of an environmental monitoring program?
Q. What is the significance of viable and non-viable particle monitoring and what is difference between them?
Q. What are the common methods for monitoring air quality in pharmaceutical cleanrooms?
Q. What is maximum permitted microbial contamination level during qualification of various grades ?
Q.5: Why only 0.5 and 5 micron particles are measured for NVPC ?
Q. What is non-viable particle count limit in various grades in pharmaceutical industry ?
Q. When we should change settle plates exposed in the area for monitoring ?
Q. What are the different methods for surface monitoring in cleanrooms?
Q. What is at rest condition and in-operation condition ?
Q. What are touch plates / RODAC plates ?
Q. In which cases Swabbing sampling technique becomes more useful ?
Q. Explain method of liquid monitoring ?
Q.What is working principle of NVPC counters ?
Q. What should be the number of sampling locations to be tested?
Q. Which guidelines are referred for environmental monitoring in pharmaceutical industry ?

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Keywords to find this video:
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