Clean room classification by particle size concentration ISO 14644-1, ISO 5, ISO 6, ISO 7, ISO 8

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#areaclassificationinpharma, #ISO14644-1, #pharmaceutical industry, #pharmaceutical, #Cleanroom, #Contaminationcontrol, #airlock, #Aseptic, #ISO5, #ISO8, #EUGMP, #ATREST, #Inoperation, #Annex1, #cleanroomclassification, #NVPC, #pharma, #usfda, #cleanroom, #aseptic, #fda, #fdaknowledge, #sterile , #USFDA, #GMP

In this video, I have discussed the clean room classification per ISO 14644-1 focused on Pharmaceutical manufacturing of Sterile products.
What is a clean room:

Clean room:
A room designed, maintained, and controlled to prevent particle(Non viable) and microbiological contamination (Viable) of drug products. Such a room is assigned and reproducibly meets an appropriate air cleanliness classification.


0:00 - Intro
0:11 - Cleanroom Classification by particle size
1:57 - What is a Cleanroom?
2:22 - What is an airlock in a clean room?
4:00 - What is the purpose of the clean room?
4:01 - Why is a clean room required in pharmaceutical manufacturing?
4:36 - What are the main sources of contamination in the clean room?
6:33 - Cleanroom classification per ISO 14644-1:2015?
6:54 - What is class 100?
9:26 - What are Grade A, Grade B, Grade C and Grade D in cleanrooms?
13:02 - What are the applications of Pharmaceutical operations by Cleanroom Grade?
13:05 - What is the room classification of the Aseptic processing area?

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