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 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 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 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 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 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 is o...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 exposure...view more

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This European Standard provides the procedure for the specific assessment required in Annex A of EN 50527-1:2010 for workers with implanted pacemakers. It offers different approaches for doing the risk assessment. The most suitable one shall be used. If the worker has other AIMDs implanted additionally, they have to be assessed separately. The purpose of the specific assessment is to determine the risk for workers with implanted pacemakers arising from exposure to electromagnetic fields at the w...view more

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This basic standard specifies the method for assessing overall exposure from all fixed radio frequency sources at a broadcast site. This assessment may be applied at any time but must be carried out when the exposure situation changes in or around this site. It plays an essential role in the coordination of different stakeholders, with respect to ensuring EMF exposure compliance in and around a broadcast site especially for equipment installed within the site.

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This basic standard specifies the method for assessing overall exposure from all fixed radio frequency sources at a broadcast site. This assessment may be applied at any time but must be carried out when the exposure situation changes in or around this site. It plays an essential role in the coordination of different stakeholders, with respect to ensuring EMF exposure compliance in and around a broadcast site especially for equipment installed within the site.

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The scope of this European Standard is to provide a procedure in order to assess the risk to workers bearing 97 one or more active implantable medical devices from exposure to electric, magnetic and electromagnetic 98 fields at a workplace. It specifies how to perform a general risk assessment and to determine whether it is 99 necessary to carry out a detailed risk assessment.

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The scope of this European Standard is to provide a general procedure in order to assess workers' exposure to electric, magnetic and electromagnetic fields in a work place to demonstrate compliance with exposure limit values and action values as stated in the Council and European Parliament Directive 2004/40/EC. 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 spec...view more

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This European Standard gives elements to establish methods for measurement and calculation of quantities associated with the assessment of human exposure to electric, magnetic and electromagnetic fields (EMF) in the frequency range from 0 Hz to 300 GHz. The major intention of this Basic Standard is to give the common background and information to relevant EMF standards. This Basic Standard cannot go into details extensively due to the broad frequency range and the huge amount of possible applica...view more

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The scope of this European Standard is to provide a general procedure in order to assess workers’ exposure to electric, magnetic and electromagnetic fields in a work place to demonstrate compliance with exposure limit values and action values as stated in the Council and European Parliament Directive 2004/40/EC. 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 spec...view more

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This product family standard applies to equipment for resistance welding, arc welding and allied processes designed for use in industrial or domestic environments, including welding power sources, wire feeders and ancillary equipment, e.g. torches, liquid cooling systems and arc striking and stabilising devices. NOTE 1 Allied processes are for example resistance hard and soft soldering, resistance heating by means comparable to resistance welding equipment, electric arc cutting and arc spraying....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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