Customer Support: +1 416-401-8730

Login to i2i Subscription Intertek.com
  • There are no items in your cart
Please enter a keyword to search
Advanced search
Home
AS
AS/NZS 3824:1998

AS/NZS 3824:1998

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.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

Available format(s)

Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users

Withdrawn date

03-30-2022

Language(s)

English

Published date

07-05-1998

Publisher

Standards Australia

1 - AS/NZS 3824:1998 GUIDELINES FOR RADIOTHERAPY TREATMENT ROOMS DESIGN
4 - PREFACE
6 - CONTENTS
7 - INTRODUCTION
9 - 1 Scope and object
9 - 1.1 Scope
9 - 1.2 Object
9 - 1.3 Collateral and Particular Standards
10 - 2 Electrical requirements
10 - 2.1 SUPPLY MAINS
10 - 2.2 Isolation from the SUPPLY MAINS
11 - 2.3 Electromagnetic compatibility
11 - 2.4 TREATMENT ROOM lighting
11 - 2.5 Electrical FIXED MAINS SOCKET-OUTLETS
11 - 3 Environmental requirements
11 - 3.1 Ventilation
12 - 3.2 Temperature, pressure and humidity requirements
12 - 3.3 Air filtration
12 - 3.4 Water supply
12 - 3.5 Cleaning requirements
13 - 3.6 Fire protection
13 - 3.7 Magnetic field
13 - 3.8 Floor covering and wall coating
13 - 4 TREATMENT ROOM entrance system
13 - 4.1 Entrance barrier system
13 - 4.2 TREATMENT ROOM entrance INTERLOCKS
14 - 5 Movable floor
14 - 6 ACCESSORIES handling and storage
15 - 7 Miscellaneous
15 - 7.1 Video and audio surveillance
15 - 7.2 PATIENT alignment system
15 - 7.3 Indicator lights and warning signs
15 - 7.4 Access ducts to the TREATMENT ROOM
16 - 8 Protection against IONIZING RADIATION outside the TREATMENT ROOM
16 - 9 Information to be given by the RADIOTHERAPY EQUIPMENT MANUFACTURER
17 - 10 Reference documents

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.

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.

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

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 specification - Medical electrical equipment - Particular requirements for safety - Remote-controlled automatically-driven gamma-ray afterloading equipment

View more information
US$34.90
Excluding Tax where applicable
USD
CAD
CHF
CNY
DKK
EUR
GBP
HKD
IDR
INR
JPY
KRW
MXN
NOK
NZD
SEK
SGD
USD
ZAR
Hardcopy - English
PDF 1 User - English
PDF 3 Users - English
PDF 5 Users - English
PDF 9 Users - English
01
02
03
04
05
06
07
08
09
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50

Access your standards online with a subscription

Features

  • Simple online access to standards, technical information and regulations.

  • Critical updates of standards and customisable alerts and notifications.

  • Multi-user online standards collection: secure, flexible and cost effective.

Learn more on subscription solutions

or

Get in touch with us