Non viable particle count in Pharmaceutical industry l Interview Questions скачать в хорошем качестве

Non viable particle count in Pharmaceutical industry l Interview Questions

Non viable particle count in Pharmaceutical industry l Interview Questions ----------------------------------------------------------------------------------------------- Go to below playlists and search for a topic you want: 1. QMS - Quality Management System in Pharmaceutical industry :    • QMS - Quality Management System in Pharmac...   2. QA- Quality assurance in Pharmaceutical industry. :    • QA- Quality assurance in Pharmaceutical in...   3. QC - Quality Control in Pharmaceutical industry :    • QC - Quality Control in Pharmaceutical ind...   4. OSD - Tablet Manufacturing in Pharmaceutical industry :    • OSD - Tablet Manufacturing in Pharmaceutic...   5. Injectable processing - Injectable processing or Sterile dosage formulation :    • Injectable processing - Injectable process...   ----------------------------------------------------------------------------------------------- Questions covered: Q.1 : What is difference between Viable and Non-viable particle count ? Q.2 : What is objective of particle monitoring in clean room ? Q.3: Which guidelines are referred for NVPC ? Q.4: What is NVPC limit for GRADE A and Grade B ? Q.5: Why only 0.5 and 5 micron particles are measured for NVPC ? Q.6: What is difference between alert limit and action limit for NVPC ? Q.7: At what rate air is measured in commercial non-viable particle counters ? Q.8 Why particle counters are needs to be ON at least 36 minutes prior to process monitoring ? Q.9: What is momentary excursion / false count ? Q.10: What should be action plan in case of repeat NVPC excursion? Q.11:What should be the isokinetic probe location? Q.12:Why zero count or purge test is done ? Q.13: What are the basic requirements for tubing’s used for particle monitoring device connection? Q.14: What is ideal sample height? Q.15: It is necessary to measure Non-viable particle count during entire batch processing? Q.16 What is working principle of NVPC counters ? Q.17 How we can control Non-viable particle counts in clean room ? Q.18 What should be the number of sampling locations to be tested? Q.19 What are the commonly used particle counters in pharmaceutical industry ? Q.20 What are the other environmental monitoring tests done in clean room ? ----------------------------------------------------------------------------------------------- Keywords to find this video: difference between Viable and Non-viable particle count,objective of particle monitoring in clean room,guidelines are referred for NVPC,NVPC limit for GRADE A and Grade B,0.5 and 5 micron particles are measured for NVPC,difference between alert limit and action limit for NVPC,working principle of NVPC counters,Non-viable particle count during entire batch processing,zero count or purge test,action plan in case of repeat NVPC excursion,isokinetic probe location ----------------------------------------------------------------------------------------------- Copyright disclaimer: “Any illegal reproduction of this content will result in immediate legal action.”