ISO area classification l ISO Guideline l Clean room classification l Question and answers

ISO Guideline for area classification l Clean room classification l Area Qualification l Interview Question and answers
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Questions covered:
Q. What is current ISO guideline for area classification?
Q. How many ISO cleanroom classes are there ?
Q. What is at rest condition and in-operation condition as per ISO ?
Q. How is air cleanliness tested according to ISO 14644-1?
Q. What are the key parameters monitored in ISO cleanrooms ?
Q. Which particle sizes are primarily measured in ISO classifications ?
Q. What is maximum allowable air cleanliness by particle concentration ?
Q. What are the ISO requirements for NVPC (Non-Viable Particle Count) report ?
Q. How much should be the sampling locations for particle counting as per ISO 14644-1 :2015 ?
Q. What is OPC limit for area classification in the pharmaceutical industry ?
Q. What are the sampling location selection requirement as per ISO?
Q. Why only 0.5 and 5 micron particles are measured during area classification ?
Q. What is basis for determination of the concentration of airborne particles as per ISO Guideline ?
Q. What is definition of clean room as per ISO Guideline ?
Q. What is unidirectional airflow as per ISO guideline ?
Q. What is requirement for test instrument used for particle monitoring as per ISO guideline ?
Q. What are the alternative guidelines for ISO area classification ?
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Keywords to find this video:
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[@dongtruong2388]

Thank so much for your information! It is so good. If you have information about “requirements in filling room guidelines” plz share or guide to me where I could find information! Thanks

[@PharmGrow]

Thanks. I will work on it 👍