AS/NZS 3824:1998
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Guidelines for radiotherapy treatment rooms design
Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
30-03-2022
English
05-07-1998
Applies to those aspects of a radiotherapy installation which ensure the safety of the patient, the equipment operator and other persons present during the period in which the equipment is in use. General construction requirements are not addressed. This Standard is identical with and has been reproduced from IEC 61859:1997.
Committee |
HE-003
|
DocumentType |
Standard
|
ISBN |
0 7337 1987 2
|
Pages |
9
|
ProductNote |
Pending Revision indicates that as a result of the Aged Standards review process, the document needs updating. If no project proposal, meeting the quality criteria, is received within the 12 month timeframe, the document shall be withdrawn.
|
PublisherName |
Standards Australia
|
Status |
Withdrawn
|
Supersedes |
This technical report applies only to those aspects of the installation ensuring the safety of the PATIENT, the OPERATOR and other persons during the RADIOTHERAPY EQUIPMENT use. General construction requirements are not addressed in this technical report. The installations considered in this technical report are those in which are located RADIOTHERAPY EQUIPMENT delivering IONIZING RADIATION used for therapeutic purpose, suchas MEDICAL ELECTRON ACCELERATORS, GAMMA BEAM THERAPY EQUIPMENT AND GAMMA-RAY AFTERLOADING EQUIPMENT. RADIOTHERAPY SIMULATOR installations are not included in thistechnical report. A particular RADIOTHERAPY EQUIPMENT installation may generally consist of several rooms, such as: - the TREATMENT ROOM in which the RADIATION BEAM is emitted and in which the PATIENT is located during the IRRADIATION, including all enclosed spaces where a person could remain inadvertently during the IRRADIATION; - the control room in which the TREATMENT CONTROL PANEL is located and from which the OPERATOR controls the IRRADIATION and other functions of the RADIOTHERAPY EQUIPMENT; - other rooms which may contain other parts of the RADIOTHERAPY EQUIPMENT, but where IRRADIATION is not carried out.
Standards | Relationship |
IEC TR 61859:1997 | Identical |
First published as AS/NZS 3824:1998
AS/NZS 3200.2.8:1994 | Medical electrical equipment Particular requirements for safety - Therapeutic X-ray generators |
AS/NZS 3200.1.2:1995 | Approval and test specification - Medical electrical equipment General requirements for safety - Collateral Standard: Electromagnetic compatibility - Requirements and tests |
AS/NZS 3200.2.17:1994 | Approval and test specifications - Medical electrical equipment Particular requirements for safety - Remote-controlled automatically-driven gamma-ray afterloading equipment |
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