AS 1807.6:2000 PDF

Scope: This Standard sets out the method for determining the overall integrity of a terminally mounted HEPA filter installation in a cleanroom, workstation, safety cabinet, or pharmaceutical isolator.

AS 1807.6:2000 Referenced Document

AS 1386.1 Cleanrooms and clean workstations - Principles of clean space control
AS 1807 Separative devices — Biological and cytotoxic drug safety cabinets, clean workstations and pharmaceutical isolators — Methods of test*， 2021-04-01 Update
AS 1807.0 Clean room, workstation, safety cabinet and drug isolator test methods method and instrument list
AS 1807.1 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of air velocity and uniformity of air velocity in clean workstations, laminar flow safety cabinets and pharmaceutical isolators
AS 1807.3 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test - Determination of air velocity in laminar flow cleanrooms
AS 1807.7 Test Methods for Cleanrooms, Workstations, Safety Cabinets, and Pharmaceutical Isolators Determination of Integrity of Non-Terminal Installed HEPA Filter Assemblies
AS 4260 High efficiency particulate air (HEPA) filters - Classification, construction and performance
AS/NZS 1716 Amendment No.1 to AS/NZS 1716-2003 Respiratory protective devices

1970 AS 1807.6:2000/Amdt 1:2002 Clean Room, Workstation, Safety Cabinet, and Pharmaceutical Isolator Test Methods Determination of Integrity of Terminal Installed HEPA Filter Assemblies
2000 AS 1807.6:2000 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test - Determination of integrity of terminally mounted HEPA filter installations