Aseptic filling area / sterile filling area l Pharmaceutical industry l Interview Questions
-----------------------------------------------------------------------------------------------
Go to below playlists and search for a topic you want:
1. QMS - Quality Management System in Pharmaceutical industry : [ Ссылка ]
2. QA- Quality assurance in Pharmaceutical industry. : [ Ссылка ]
3. QC - Quality Control in Pharmaceutical industry : [ Ссылка ]
4. OSD - Tablet Manufacturing in Pharmaceutical industry : [ Ссылка ]
5. Injectable processing - Injectable processing or Sterile dosage formulation : [ Ссылка ]
-----------------------------------------------------------------------------------------------
Questions covered:
Q.1 : In which Area / class aseptic filling is done ?
Q.2: What should be the supporting area for filling room ?
Q.3: When we should do environmental monitoring during aseptic processing ?
Q.4 : What is aseptic filling ?
Q.5: Which Guidelines are referred for aseptic filling process
Q.6 What should be the dosing accuracy of vial /ampoule filling machine ?
Q.7: When we should Qualify Vial / Ampoule Filling machine ?
Q.8: When we should perform filling after completion of filtration process ?
Q.9: Why nitrogen gas is used for purging and overlaying in glass vials ?
Q.10: How you will ensure sterility Assurance level of aseptic filling process ?
Q.11: What is use of buffer tank / buffer vessel during aseptic filling ?
Q.12 What are the Qualification tests for filling machine ?
-----------------------------------------------------------------------------------------------
Keywords to find this video:
single use filling,vial filling machine,sterile area,ampoule filling machine,filling machine,aseptic process simulation,sterility assurance,aseptic processing,aseptic practice,pharmaceutical industry,us fda guidelines,fill finish,sterilization,sterile,us fda quality assurance,data integrity,us fda in india,aseptic,final filtration,particles,final fill,you have been warned,us fda auditor,us fda in pharmaceuticals,quality management,training,us fda 483
-----------------------------------------------------------------------------------------------
Copyright disclaimer:
“Any illegal reproduction of this content will result in immediate legal action.”
Ещё видео!