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ISO 17751-1:2016 specifies a method for the identification, qualitative, and quantitative analysis of cashmere, wool, other speciality animal fibres, and their blends using light microscopy (LM).ISO 17751-1:2016 is applicable to loose fibres, intermediate-products, and final products of cashmere, wool, other speciality animal fibres, and their blends.

This part of ISO 17751 specifies a method for the identification, qualitative and quantitative analysis of cashmere, wool, other specialty animal fibres, and their blends using light microscopy (LM). This part of ISO 17751 is applicable to loose fibres, intermediate-products, and final products of cashmere, wool, other specialty animal fibres, and their blends.

This part of ISO 17751 specifies a method for the identification, qualitative, and quantitative analysis of cashmere, wool, other specialty animal fibres, and their blends using scanning electron microscopy (SEM). This part of ISO 17751 is applicable to loose fibres, intermediate products, and final products of cashmere, wool, other specialty animal fibres, and their blends.

This document specifies average values of leather density, depending on animal origin and thickness of finished leather, to be used for the calculation of LCA. This document is applicable to bovine, caprine and ovine types of leather, except for vegetable sole leather, which is traded by weight.

This document is applicable to new manufactured tags after publication of this document.This document aims to:- provide specification for RFID tag manufacturers to design and manufacture passive UHF RFID tags for the aeronautical industry;- identify required performances for UHF RFID tags in order to be read/written during ground operations only, while being subject to the global flight environment;- identify functional and environmental validation tests to be performed on passive UHF RFID tags with associated pass/fail criteria as well as associated test methods;- check functionalities and resistance to environment for airborne passive UHF RFID tags.This document does not cover:- the reader (interrogator - readers). It will be addressed appropriately by individual applicants;- active RFID devices or battery assisted passive (BAP) RFID devices;- RFID tags designed to operate outside the 860 to 960 MHz frequency range.

This document is applicable in the aeronautical domain to on-board parts and to equipment intended to be embedded or positioned on any civil or military airborne vehicle with a type certificate.The purpose of this document is to guide design, manufacturing, maintenance and operations organizations in the installation, removal and replacement of RFID tags (UHF and HF) and Contact Memory Buttons (CMB), according to the environments defined in RTCA DO-160/EUROCAE ED-14 and according to the type of support and the expected fixation performances. This guide will provide help in the specification of the tag installation/removal functions and/or will enable the solutions on offer from tag suppliers to be enhanced.The term "tag" used in this document covers all the tags used to store electronic data, including RFID tags and CMB tags. As a reminder, the tags can also contain information that can be read by devices other than RFID or CMB readers (e.g., bar codes - Data Matrix, QR codes, etc., and/or alphanumerical characters) and information that can be read by the naked eye without any tools (human-readable).

This document specifies minimum requirements of performance characteristics for the detection of nucleic acid sequences (DNA) by molecular methods, such as the polymerase chain reaction (PCR), including different post-PCR detection methods, real-time PCR, single and/or multiple probe-based detection techniques as well as the combination of such methods.The document is applicable to the detection, identification and quantification of DNA from animal species of higher and lower taxonomic groups in foodstuffs, and the validation of applicable methods.It is applicable to mammals, birds, reptiles, amphibians, fishes, molluscs, crustaceans and insects. Typical examples for each are listed in Annex A.

This European Standard specifies a test method simulating practical conditions for establishing whether aproduct for hygienic handrub reduces the release of virus contamination on hands when rubbed onto theartificially contaminated hands of volunteers.NOTE 1 Attention is drawn to the fact that tests on human volunteers are the subject of legal provisions incertain European countries/regions.This European Standard applies to products for hygienic handrub for use in areas and situations wheredisinfection is medically indicated. Such indications occur in patient care, for example:– in hospitals, in community medical facilities and in dental institutions;– in clinics of schools, of kindergardens and of nursing homes.and may occur in the workplace and in the home. It may also include services such as laundries and kitchenssupplying products directly for the patient.EN 14885 specifies in detail the relationship of the various tests to one another and to “use recommendations”.NOTE 2 This method corresponds to a phase 2, step 2 test.

This document specifies performance requirements for voice prostheses including requirements for marking, packaging and information to be provided by the manufacturer as well as test methods for the evaluation of physical characteristics of voice prostheses.NOTE      There is guidance or rationale for this list item contained in A.2.

The purpose of this document is to provide minimum criteria required for quality assurance and quality control, evaluation of the performance and to facilitate the comparison of measurements related to absorbed dose estimation obtained in different laboratories applying ex vivo X-band EPR spectroscopy with human tooth enamel.This document covers the determination of absorbed dose in tooth enamel (hydroxyapatite). It does not cover the calculation of dose to organs or to the body.This document addresses:a) responsibilities of the customer and laboratory;b) confidentiality and ethical considerations;c) laboratory safety requirements;d) the measurement apparatus;e) preparation of samples;f) measurement of samples and EPR signal evaluation;g) calibration of EPR dose response;h) dose uncertainty and performance test;i) quality assurance and control.

This document focuses on monitoring the activity concentrations of radioactive gases. They allow the calculation of the activity releases, in the gaseous effluent discharge from facilities producing positron emitting radionuclides and radiopharmaceuticals. Such facilities produce short-lived radionuclides used for medical purposes or research and can release gases typically including, but not limited to 18F, 11C, 15O and 13N. These facilities include accelerators, radiopharmacies, hospitals and universities. This document provides performance-based criteria for the design and use of air monitoring equipment including probes, transport lines, sample monitoring instruments, and gas flow measuring methods. This document also provides information on monitoring program objectives, quality assurance, development of air monitoring control action levels, system optimisation and system performance verification.The goal of achieving an unbiased measurement is accomplished either by direct (in-line) measurement on the exhaust stream or with samples extracted from the exhaust stream (bypass), provided that the radioactive gases are well mixed in the airstream. This document sets forth performance criteria and recommendations to assist in obtaining valid measurements.NOTE 1 The criteria and recommendations of this document are aimed at monitoring which is conducted for regulatory compliance and system control. If existing air monitoring systems were not designed according to the performance criteria and recommendations of this document, an evaluation of the performance of the system is advised. If deficiencies are discovered based on a performance evaluation, a determination of the need for a system retrofit is to be made and corrective actions adopted where practicable.NOTE 2 The criteria and recommendations of this document apply under both normal and off-normal operating conditions, provided that these conditions do not include production of aerosols or vapours. If the normal and/or off-normal conditions produce aerosols and vapours, then the aerosol collection principles of ISO 2889 also apply.

This document specifies minimum nuclear criticality safety training requirements for operations staff, operations supervisors, and management.This document is applicable to areas, processes or facilities containing quantities of fissile material for which nuclear criticality safety assessment is required as defined in ISO 1709.This document is not applicable to the transport of fissile materials outside the boundaries of nuclear establishments.

This document specifies the different leakage test methods for sealed sources. It gives a comprehensive set of procedures using radioactive and non-radioactive means.This document applies to the following situations:— leakage testing of test sources following design classification testing in accordance with ISO 2919[1];— production quality control testing of sealed sources;— periodic inspections of the sealed sources performed at regular intervals, during the working life.Annex A of this document gives guidance to the user in the choice of the most suitable method(s) according to situation and source type.It is recognized that there can be circumstances where special tests, not described in this document, are required.It is emphasized, however, that insofar as production, use, storage and transport of sealed radioactive sources are concerned, compliance with this document is no substitute for complying with the requirements of the relevant IAEA regulations[17] and other relevant national regulations. It is also recognized that countries can enact statutory regulations which specify exemptions for tests, according to sealed source type, design, working environment, and activity (e.g., for very low activity reference sources where the total activity is less than the leakage test limit).

The primary purpose of this document is to provide minimum acceptable criteria required to establish a procedure for retrospective dosimetry by electron paramagnetic resonance spectroscopy and to report the results.The second purpose is to facilitate the comparison of measurements related to absorbed dose estimation obtained in different laboratories.This document covers the determination of absorbed dose in the measured material. It does not cover the calculation of dose to organs or to the body. It covers measurements in both biological and inanimate samples, and specifically:a) based on inanimate environmental materials like glass, plastics, clothing fabrics, saccharides, etc., usually made at X-band microwave frequencies (8 GHz to 12 GHz);b) in vitro tooth enamel using concentrated enamel in a sample tube, usually employing X-band frequency, but higher frequencies are also being considered;c) in vivo tooth dosimetry, currently using L-band (1 GHz to 2 GHz), but higher frequencies are also being considered;d) in vitro nail dosimetry using nail clippings measured principally at X-band, but higher frequencies are also being considered;e) in vivo nail dosimetry with the measurements made at X-band on the intact finger or toe;f) in vitro measurements of bone, usually employing X-band frequency, but higher frequencies are also being considered.For biological samples, in vitro measurements are carried out in samples after their removal from the person or animal and under laboratory conditions, whereas the measurements in vivo are carried out without sample removal and may take place under field conditions.NOTE The dose referred to in this document is the absorbed dose of ionizing radiation in the measured materials.

This document specifies minimum requirements for life rafts carried on helicopters operating in a hostile sea area or over very rough sea conditions. Life rafts covered by this document are for use by helicopter crew members and passengers in the event of a ditching or water impact.They are intended either for integration into the helicopter, or stowed in the cabin before being manhandled out of the helicopter. This document does not cover air-drop life rafts.

This document specifies a method for the determination of the breaking and immediate adhesivity behaviour of cationic bituminous emulsions in contact with aggregate. The method applies to emulsions used for surface dressing and similar applications and can be used for formulation as well as for production control purposes.WARNING — The use of this document can involve hazardous materials, operations and equipment. This document does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this document to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

This document specifies safety requirements within the meaning of Directive 42/2006/EC, "Machinery Directive".The deviations from EN 17206 specified in this part are based on the particular operating conditions for stands and cannot be applied to other machinery installations.This document applies to manually operated and/or power-driven stands with an Entertainment Load Limit [ELL] of more than 3 kg.NOTE 1: The ELL is the maximum load that an item of lifting equipment is designed to raise, lower or sustain.This document applies to stands which are used in places of assembly and in staging and production facilities for events and theatrical productions.Stands within the scope of this document are used for the purposes of lifting, lowering and holding loads (e.g. scenic elements, trusses, lighting and audiovisual equipment). It is also possible for several stands to carry a common load.This document does not cover installations that are used for the transportation of persons or for the movement of loads above people’s heads.This document only covers installations with people under the load when the installations are at rest.NOTE 2: During setup, the operator can, for operational reasons, be required to stand under the moving load for short periods of time.This document also applies to installations with new technologies or customized designs that are not expressly named here but are being used in identical modes of operation.This document does not apply to:- stands with a Load Limit = 3 kg;- camera stands;- wooden stands.This document also specifies the information to be communicated between manufacturers and users, and the details that are to be provided with regard to the intended use of the machinery installations.The significant hazards dealt with in this document are identified in Clause 4.

This European Standard specifies the requirements and gives recommendations for the design, sizing, installation, identification, commissioning and maintenance of rainwater harvesting systems for the use of rainwater on-site as non-potable water. This European Standard also specifies the minimum requirements for these systems.Excluded from the scope of this European Standard are:- the use as drinking water and for food preparation;- the use for personal hygiene purposes;- decentralized attenuation;- infiltration.NOTE Conformity with the standard does not exempt from compliance with the obligations arising from local or national regulations.