AS 1807.6-2000
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of integrity of terminally mounted HEPA filter installations
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25-07-2024
15-02-2000
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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.
| Committee |
ME-060
|
| DocumentType |
Standard
|
| ISBN |
0 7337 3219 4
|
| Pages |
3
|
| PublisherName |
Standards Australia
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
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.NOTE: A test method for determination of the overall integrity of HEPA filter installations which are not terminally mounted is specified in AS 1807.7.
First published as AS 1807.6-1976.
Second edition 1989.
Third edition 2000.
| AS 4260-1997 | High efficiency particulate air (HEPA) filters - Classification, construction and performance (Reconfirmed 2018) |
| AS 1807.0-2000 | Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test List of methods and apparatus |
| AS 1807.3-2000 | Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of air velocity in laminar flow cleanrooms |
| AS 1807.1-2000 | 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 1807.7-2000 | Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of integrity of HEPA filter installations not terminally mounted |
| AS/NZS 1716:2003 | Respiratory protective devices |
| AS 1386.1-1989 | Cleanrooms and clean workstations - Principles of clean space control |
| AS/NZS 2243.3:2002 | Safety in laboratories Microbiological aspects and containment facilities |
| AS 2252.1-2002 | Biological safety cabinets - Biological safety cabinets (Class I) for personnel and environment protection |
| AS 2252.2-2004 | Biological safety cabinets - Laminar flow biological safety cabinets (Class II) for personnel, environment and product protection |
| AS 1807.7-2000 | Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of integrity of HEPA filter installations not terminally mounted |
| AS 2567-2002 | Laminar flow cytotoxic drug safety cabinets |
| AS 2252.6-2011 | Controlled environments Clean workstations - Design, installation and use |
| AS 2252.2-2009 | Controlled environments Biological safety cabinets Class II - Design |
| HB 260-2003 | Hospital acquired infections - Engineering down the risk |
| AS 1386.5-1989 | Cleanrooms and clean workstations - Clean workstations |
| AS/NZS 2243.3:2010 | Safety in laboratories Microbiological safety and containment |
| AS 1807.5-2000 | Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of work zone integrity |
| AS 2252.5:2017 | Controlled environments Cytotoxic drug safety cabinets (CDSC) - Design, construction, installation, testing and use |
| AS 1324.2-2003 | Air filters for use in general ventilation and airconditioning Methods of test |
| AS 1386.7-1989 | Cleanrooms and clean workstations - Installation and use of clean workstations |
| AS 1807.22-2000 | Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of air barrier containment of laminar flow safety cabinets |
| AS 1386.3-1989 | Cleanrooms and clean workstations - Non-laminar flow cleanrooms - Class 350 and cleaner |
| AS 1386.2-1989 | Cleanrooms and clean workstations - Laminar flow cleanrooms |
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