European standard establishes the procedures and methodology on measurement and calculation of quantities associated with the assessment of human exposure to electric, magnetic and electromagnetic fields in the frequency range from 0 Hz to 300 GHz. It deals with quantities that can be measured or calculated in free space, notably electric and magnetic field strength and includes the measurement and calculation of quantities inside the body that forms the basis for protection guidelines.
In part...
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TThe scope of this European Standard is to provide a general procedure for the assessment of workers’ exposure to electric, magnetic and electromagnetic fields in a workplace in order to determine compliance with exposure limit values and/or action levels as stated in European Directive 2013/35/EU
The purpose of this European Standard is to
-   specify how to perform an initial assessment of the levels of workers' exposure to electromagnetic fields (EMF), if necessary including specific exposure...
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This document provides general methods for measurement and calculation of quantities associated with human exposure to electromagnetic fields in the frequency range from 0 Hz to 300 GHz. It is intended specifically to be used for the assessment of emissions from products and comparison of these with the exposure limits for the general public given in Council Recommendation 1999/519/EC, and those given for workers in Directive 2013/35/EU, as appropriate. It also is intended to be used for assessm...view more

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The scope of this document is to provide a general procedure for the assessment of workers’ exposure to electric, magnetic and electromagnetic fields in a workplace in order to determine compliance with exposure limit values and/or action levels as stated in European Directive 2013/35/EU. The purpose of this document is to — specify how to perform an initial assessment of the levels of workers' exposure to electromagnetic fields (EMF), if necessary, including specific exposure assessment of such...view more

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This part of IEC 62822, which is a product family standard, applies to equipment for
resistance welding, arc welding and allied processes designed for occupational use by
professionals and for use by laymen.
NOTE 1 Typical allied processes are resistance hard and soft soldering, resistance heating by means comparable
to resistance welding equipment, electric arc cutting and arc spraying.
The frequency range covered is 0 Hz to 300 GHz.
This product family standard specifies assessment metho...
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IEC 62822-1:2016 is a product family standard, applies to equipment for resistance welding, arc welding and allied processes designed for occupational use by professionals and for use by laymen.

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This International Standard specifies requirements for strong points for attaching chains, cables and lines for
anchoring, mooring and towing small craft. It does not specify the requirement for any strong point from which
the craft can tow other vessels. This standard is applicable to small craft with a hull length up to 24 m.
This International Standard does not define anchor weights or the length of chains and lines.

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This European Standard provides the procedure for the specific assessment required in Annex A of EN 50527 1:2015 for workers with implanted cardioverter defibrillators. It offers different approaches for doing the risk assessment. The most suitable one shall be used. If the worker has other Active Implantable Medical Devices (AIMDs) implanted additionally, they have to be assessed separately.

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This standard provides methods for assessing compliance with the requirements of the Directive 2013/35/EU] at a site operating one or more broadcast transmitters.
This standard covers the frequency range up to 40 GHz.
NOTE   The Council and European Parliament Directive 2013/35/EU will be transposed into national legislation in all the EU member countries. Users of this standard shall consult the national legislation related to this transposition in order to identify the national regulations and...
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This European Standard provides the procedure for the specific assessment required in Annex A of EN 50527 1:2015 for workers with implanted cardioverter defibrillators. It offers different approaches for doing the risk assessment. The most suitable one shall be used. If the worker has other Active Implantable Medical Devices (AIMDs) implanted additionally, they have to be assessed separately.

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This European standard provides methods for assessing compliance with the requirements of the Directive 2013/35/EU] at a site operating one or more broadcast transmitters. This standard covers the frequency range up to 40 GHz. NOTE The Council and European Parliament Directive 2013/35/EU will be transposed into national legislation in all the EU member countries. Users of this standard shall consult the national legislation related to this transposition in order to identify the national regulati...view more

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The object of this generic standard is to provide a route for evaluation of such equipment against limits on human exposure to electric, magnetic and electromagnetic fields, and induced and contact current.
This standard applies to electronic and electrical equipment for which no dedicated product- or product family standard, or standard relating to low power equipment,  regarding human exposure to electromagnetic fields exists. If such a standard does exist then it shall be used and this stan...
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The object of this generic standard is to provide a route for evaluation of equipment used by workers against limits on human exposure to electric, magnetic and electromagnetic fields, and induced and contact current  when it is put into service in its operational environment, and also for in situ or post-market evaluation of such equipment
The frequency range covered is 0 Hz to  300 GHz.
The requirement for this standard arises from the withdrawal of EMF standardisation mandate M/305 and its ...
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The object of this generic standard is to provide a route for evaluation of such equipment against limits on human exposure to electric, magnetic and electromagnetic fields, and induced and contact current. This standard applies to electronic and electrical equipment for which no dedicated product- or product family standard, or standard relating to low power equipment, regarding human exposure to electromagnetic fields exists. If such a standard does exist then it shall be used and this standar...view more

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The object of this generic standard is to provide a route for evaluation of equipment used by workers against limits on human exposure to electric, magnetic and electromagnetic fields, and induced and contact current when it is put into service in its operational environment, and also for in situ or post-market evaluation of such equipment. The frequency range covered is 0 Hz to 300 GHz. Other standards can apply to products covered by this document. In particular this document is not designed t...view more

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This European standard provides simple conformity assessment methods for low-power electronic and electrical equipment operating at frequencies between 10 MHz and 300 GHz to an electromagnetic field (EMF) exposure limit. If such equipment cannot be shown to comply with the applicable EMF exposure requirements using the exposure assessment methods in this standard, then other EMF product standards may be used for conformity assessment. Other standards can apply to products covered by this documen...view more

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This European Standard provides a general procedure to assess workers’ exposure to electric and magnetic fields (EMF) in work places associated with the production, transmission and distribution of electric energy, and to demonstrate compliance with exposure limit values and action levels as stated in the Council and European Parliament “EMF” Directive 2013/35/EU [10].
It has the role of a specific workplace standard. It takes into account the non-binding application guide for implementing the ...
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This European Standard provides a general procedure to assess workers’ exposure to electric and magnetic fields (EMF) in work places associated with the production, transmission and distribution of electric energy, and to demonstrate compliance with exposure limit values and action levels as stated in the Council and European Parliament "EMF" Directive 2013/35/EU [12]. NOTE 1 The Council and European Parliament Directive 2013/35/EU will be transposed into national legislation in all the EU membe...view more

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This European Standard provides the procedure for the specific assessment required in EN 50527-1:2016,
Annex A, for workers with implanted pacemakers. It offers different approaches for doing the risk
assessment. The most suitable one will be used. If the worker has other Active Implantable Medical Devices
(AIMDs) implanted additionally, they need to be assessed separately.
The purpose of the specific assessment is to determine the risk for workers with implanted pacemakers
arising from exp...
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This European Standard provides a procedure to assess the risk to workers bearing one or more active
implantable medical devices from exposure to electric, magnetic and electromagnetic fields at a workplace. It
describes how a general risk assessment should be performed and determines whether it is necessary to
carry out a detailed risk assessment.
NOTE 1 This European Standard does not cover indirect effects caused by non active implants.
NOTE 2 The risk of human exposure to EMF considered...
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This European Standard provides the procedure for the specific assessment required in EN 50527-1:2016, Annex A, for workers with implanted pacemakers. It offers different approaches for doing the risk assessment. The most suitable one will be used. If the worker has other Active Implantable Medical Devices (AIMDs) implanted additionally, they need to be assessed separately. The purpose of the specific assessment is to determine the risk for workers with implanted pacemakers arising from exposure...view more

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This European Standard provides a procedure to assess the risk to workers bearing one or more active implantable medical devices from exposure to electric, magnetic and electromagnetic fields at a workplace. It describes how a general risk assessment should be performed and determines whether it is necessary to carry out a detailed risk assessment. NOTE 1 This European Standard does not cover indirect effects caused by non active implants. NOTE 2 The risk of human exposure to EMF considered is o...view more

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This European Standard provides the procedure for the specific assessment required in Annex A of EN 50527 1:2015 for workers with implanted neurostimulators (e.g. spinal cord, deep-brain, retinal, bladder). It offers different approaches for doing the risk assessment. The most suitable one shall be used. If the worker has other Active Implantable Medical Devices (AIMDs) implanted additionally, they have to be assessed separately.

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This document provides the procedure for the specific assessment required in EN 50527 1:2016, Annex A, for workers with implanted neurostimulator systems (NS), specifically of the type used for spinal cord stimulation (SCS). It is recognized that implantable neurostimulators have been developed for a wide variety of clinical applications, however the SCS devices within the scope of this document represent the largest segment of the implantable neurostimulator applications thus far. NOTE 1 If the...view more

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