This document specifies a test method for the determination of the content of chlorophenol-based preservative agents in textile materials and articles composed of textile products, by chromatography.

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This document specifies test methods and performance requirements for alcohol interlocks having a mouthpiece. It covers alcohol interlocks to be used in all general preventive programmes and those for drink driving offenders and legally regulated programmes monitored or controlled in a comparable way.
This document can also be used for alcohol interlocks intended for other applications.
This document is directed at test laboratories and manufacturers of alcohol interlocks. It defines requirements and test procedures for type testing.
Several parameters (such as alcohol concentration or breath volume) are specified in this document for the purpose of type testing according to this document only. However, it can be necessary due to national regulations or depending on user requests to set the values of the prescribed parameters differently when the alcohol interlocks are in use.
This document also applies to alcohol interlocks integrated into other control systems of the vehicle as well as to accessory devices connected to the alcohol interlock.
This document does not apply to
—   instruments measuring the alcohol concentration in the ambient air in the vehicle,
—   alcohol interlocks not having a mouthpiece,
—   methods of installation and connections to the vehicle.

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X-ray Fluorescence Spectrometry (XRF) has been used for several decades as an important analytical tool for production analysis. XRF is characterised by its speed and high precision over a wide concentration range and since the technique in most cases is used as an relative method the limitations are often connected to the quality of the calibration samples. The technique is well established and most of its physical properties are well known.

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This European Standard is a product specification, giving performance requirements for fire safety cabinets to be used for the storage of flammable liquids. It is applicable to cabinets with a total internal volume of not greater than 2 m³, which may be free standing, restrained to a wall or mounted on plinth or castors.
It is not applicable to brick enclosures or walk-in storage rooms.
This Standard does not apply to any support frame or mechanism other than the base which is integral to the cabinet.
Requirements are given in respect of the construction of the cabinet and its capacity to resist fire conditions on the outside. A classification of cabinets is given, according to the level of fire resistance offered, and a type test is included, see Annex A.
The tests described in this European Standard are type tests.
This European Standard does not discriminate between different flammable liquids, which may have considerably different physical properties.
Attention is drawn to national regulations, which may apply with regards to the storage of flammable liquids.

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IEC 61010-2-034:2023 specifies safety requirements to equipment for measuring insulation resistance and to equipment for testing electric strength which have an output voltage exceeding 50 V a.c. or 120 V d.c. This document also applies to combined measuring equipment which has an insulation resistance measurement function or an electric strength test measurement function. This document has the status of a horizontal publication in accordance with IEC Guide 108. It has the status of a group safety publication in accordance with IEC Guide 104. This second edition cancels and replaces the first edition published in 2017. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
a) in 1.2.1, requirements for protection against hazards which could occur from reading a voltage have been added to the scope;
b) Clause 2, all normative references have been dated; new normative references have been added;
c) in 4.3.2.5, requirements for power supply have been modified;
d) in 4.3.2.6, requirements for inputs/outputs have been modified;
e) in 5.1.5.101.2, minimum ratings for voltage of measuring terminals are required;
f) in 5.4.2, new ratings for documentation have been added;
g) in 5.4.4, new instructions for operation have been added;
h) in 5.101.1, hazard indicators shall be functional in normal condition and in single fault condition;
i) in 6.6.101.1, insulating material of group I may be allowed for determination of creepage distances of measuring circuit terminals;
j) in 6.6.101.2, Clearances and creepage distances above 1 000 V a.c. and 1 500 V d.c. for measuring circuit terminals in unmated position have been defined;
k) in 6.6.101.3, requirements for measuring circuit terminals in partially mated position have been specified;
l) in 6.6.101.4, requirements for measuring circuit terminals in mated position have been specified;
m) Subclause 6.102 replaces 6.9.103 and has been rephrased;
n) new Subclause 9.101 to consider the protection of measuring circuits against the spread of fire and arc flash has been added. Table 102 has been replaced by Table K.101;
o) In 9.101.2, relocation of 101.3 of previous edition;
p) In 9.101.3, relocation of 101.4 of previous edition, extension to measurement category II and reference to IEC 61000-4-5 for tests;
q) in 9.101.4, requirements for measuring circuit terminals in mated position have been specified;
r) in 9.101.5, relocation of K.103 of previous edition with numerous technical changes;
s) in 14.101, relocation of 14.102. 14.101 of previous edition has been removed;
t) in 101.3, relocation of 101.5 of previous edition, and more requirements added against hazard occurring from reading a voltage value;
u) in K.2.1, another method for determination of clearances of secondary circuits is proposed;
v) in K.3.2, new Table K.15 and Table K.16 for clearance calculation;
w) in K.3.101, relocation of 6.9.104 of previous edition;
x) in K.101.4.1, new Table K.103 and Table K.104 replace Table K.102, Table K.103 and Table K.104;
y) in K.101.4, the subclause has been reviewed. Tables and tests for solid insulation have been modified. Table K.105 replaces Table K.9;
z) Table K.101, replacement of Table K.106;
aa) Clause K.4, redraft of the clause to propose a method for determination of Ut for circuits which reduce transient overvoltages;
bb) Annex EE: addition of a new informative annex for determination of clearances for Table 101.

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This document specifies test methods and performance requirements for alcohol interlocks having a mouthpiece. It covers alcohol interlocks to be used in all general preventive programmes and those for drink driving offenders and legally regulated programmes monitored or controlled in a comparable way. This document can also be used for alcohol interlocks intended for other applications. This document is directed at test laboratories and manufacturers of alcohol interlocks. It defines requirements and test procedures for type testing. Several parameters (such as alcohol concentration or breath volume) are specified in this document for the purpose of type testing according to this document only. NOTE It can be necessary due to national regulations or depending on user requests to set the values of the prescribed parameters differently when the alcohol interlocks are in use. This document also applies to alcohol interlocks integrated into control systems of the vehicle as well as to accessory devices connected to the alcohol interlock. This document does not apply to - instruments measuring the alcohol concentration in the ambient air in the vehicle, - alcohol interlocks not having a mouthpiece, - methods of installation and connections to the vehicle.

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This document is a product specification, giving performance requirements for fire safety storage cabinets to be used for the storage of flammable liquids. It is applicable to cabinets with a total internal volume of not greater than 2 m3, which can be free standing, restrained to a wall or mounted on plinth or castors.
This document does not apply to brick enclosures or walk-in storage rooms.
This document does not apply to any support frame or mechanism other than the base which is integral to the fire safety storage cabinet.
Requirements are given in respect of the construction of the fire safety storage cabinet and its capacity to resist fire conditions on the outside. A classification of fire safety storage cabinets is given, according to the level of fire resistance offered, and a type test is included, see Annex A.
The tests described in this document are type tests.
This document does not discriminate between different flammable liquids, which can have considerably different physical properties.
Attention is drawn to national regulations, which can apply with regard to the storage of flammable liquids.

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This document defines terms for surface chemical analysis. It covers general terms and those used in spectroscopy, while ISO 18115‑2 covers terms used in scanning-probe microscopy and ISO 18115‑3 covers terms used in optical interface analysis.

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This document specifies recommendations for single-phase certified reference materials (CRMs) used in electron probe microanalysis (EPMA). It also provides guidance on the use of CRMs for the microanalysis of flat, polished specimens. It does not cover organic or biological materials. This document supplements ISO 17034. A producer of CRM must also comply with ISO 17034. In case of conflict, ISO 17034 takes precedence.

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ISO 13132:2011 specifies requirements and tests for glass Petri dishes intended for general laboratory purposes and microbiological work.

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This document specifies requirements and tests for glass Petri dishes intended for general laboratory purposes and microbiological work.

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This document specifies requirements and tests for glass Petri dishes intended for general laboratory purposes and microbiological work.

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“This document specifies requirements for borosilicate 3,3 glass tubing according to ISO 3585 for laboratory apparatus in an outer diameter range from 4 mm to 300 mm. This document defines dimensions, material, denomination, designation, requirements and inspection methods.” (Scope of ISO 4803:2021)

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This document specifies requirements for borosilicate 3,3 glass tubing according to ISO 3585 for laboratory apparatus in an outer diameter range from 4 mm to 300 mm. This document defines dimensions, material, denomination, designation, requirements and inspection methods.

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This aim of this standard is to provide a process for the determination of mercury in cosmetics by means of cold vapour atomic adsorption (AAS) after pressure digestion.
The procedure was validated in 2015 by means of a multi laboratory study in combination with cold vapour AAS determination process for mercury with eight laboratories participating. Overall, seven samples representing different matrices (lipstick, tattoo colourant, body lotion, toothpaste, eyeshadow and water make-up) with varying mercury contents between 0,110 mg/kg and 5,84 mg/kg were analysed.

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This document specifies a method for quantitative determination of the concentration of selected alcohols with low boiling point in liquid waste and pasty waste by gas chromatography with flame ionization detection after static headspace extraction.
Under the conditions specified in this document, a limit of application of 20 mg/kg, expressed on dry matter for pasty waste and expressed on raw waste for liquid waste, can be achieved.

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This European Standard specifies a method for quantitative determination of 16 polycyclic aromatic hydrocarbons (PAH) (see Table ) in soil, sludge, sediment, treated biowaste, and waste, using GC-MS and HPLC-UV-DAD/FLD covering a wide range of PAH contamination levels (see Table 2).
When using fluorescence detection, acenaphthylene cannot be measured.
Table  —Target analytes of this European Standard
Target analyte   CAS-RNa
Naphthalene   91–20–3
Acenaphthene   83–32–9
Acenaphthylene   208–96–8
Fluorene   86–73–7
Anthracene   120–12–7
Phenanthrene   85–01–8
Fluoranthene   206–44–0
Pyrene   129–00–0
Benz[a]anthracene   56–55–3
Chrysene   218–01–9
Benzo[b]fluoranthene   205–99–2
Benzo[k]fluoranthene   207–08–9
Benzo[a]pyrene   50–32–8
Indeno[1,2,3-cd]pyrene   193–39–5
Dibenz[a,h]anthracene   53–70–3
Benzo[ghi]perylene   191–24–2
a   CAS-RN Chemical Abstracts Service Registry Number.
The limit of detection depends on the determinants, the equipment used, the quality of chemicals used for the extraction of the sample and the clean-up of the extract
Under the conditions specified in this European Standard, lower limit of application from 10 μg/kg (expressed as dry matter) for soils, sludge and biowaste to 100 μg/kg (expressed as dry matter) for solid waste can be achieved. For some specific samples (e.g. bitumen) the limit of 100 μg/kg cannot be reached.
Sludge, waste and treated biowaste may differ in properties as well as in the expected contamination levels of PAH and presence of interfering substances. These differences make it impossible to describe one general procedure. This European Standard contains decision tables based on the properties of the sample and the extraction and clean-up procedure to be used.
The method may be applied to the analysis of other PAH not specified in the scope, provided suitability is proven by proper in-house validation experiments.

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This document specifies the characteristics of fume cupboards, as defined in EN 14175-1, for work with unsealed radioactive materials with specific requirements regarding radiation protection. It does not apply to fume cupboards, glove boxes or hot cells (shielded radiation containment cells which can incorporate fume extraction).
The purpose of this document is to set out rules for the design and testing of fume cupboards for work with unsealed radioactive materials, in order to provide guidelines for the manufacturer, planner, installer, operator, assessor and the authorities.
This document only covers bench type fume cupboards.

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This document applies to an articulated extraction arm used as a local exhaust device in laboratories and comprised of a capture device (receiving, enclosing or capture hood, nozzle or flat screen) connected to an extraction arm which is articulated ducting to move air from the capture device to discharge.
This standard specifies:
- a method for type testing;
- a method to assess the three-dimensional capture zone of local exhaust devices mounted on an articulated extract arm;
- a method for assessing the emission release capture efficiency of local exhaust devices connected to an articulated extract arm and its robustness to a challenge of air disturbance directly in front of and in close proximity to the capture hood and release source;
- a method for establishing the reachable, three-dimensional workspace of local exhaust devices mounted on an articulated extract arm by measuring the possible positions of the opening of the device;
- a method for measuring the pressure drop and noise level in the type test;
- instructions for marking the device and recommended content of information for use;
- guidance for use describing the limitations of local exhaust devices with articulated extract arm for different airflow rates establishing the capture zone;
- guidance on selection, installation, commissioning, and control testing of articulated extract arms and their local exhaust ventilation systems.
The scope does not include filtration requirements and impact of fully or partly recirculation of the airflow extracted by an articulated extract arm.

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This document specifies requirements for the seamless integration with other microfluidic components and systems to facilitate the process of designing new microfluidic devices (e.g. microfluidic chips, sensors, actuators, connectors).
This document is applicable to devices in the field of “microfluidics” needing microfluidic interconnections.

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This document describes a method for determining the minimum detectability of surface plasmon resonance device. This document is applicable to surface plasmon resonance devices of the white-light illumination type and the laser illumination type with the angle scanning capability.

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This document specifies requirements for the seamless integration with other microfluidic components and systems to facilitate the process of designing new microfluidic devices (e.g. microfluidic chips, sensors, actuators, connectors).
This document is applicable to devices in the field of “microfluidics” needing microfluidic interconnections.

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This document applies to an articulated extraction arm used as a local exhaust device in laboratories and comprised of a capture device (receiving, enclosing or capture hood, nozzle or flat screen) connected to an extraction arm which is articulated ducting to move air from the capture device to discharge.
This standard specifies:
- a method for type testing;
- a method to assess the three-dimensional capture zone of local exhaust devices mounted on an articulated extract arm;
- a method for assessing the emission release capture efficiency of local exhaust devices connected to an articulated extract arm and its robustness to a challenge of air disturbance directly in front of and in close proximity to the capture hood and release source;
- a method for establishing the reachable, three-dimensional workspace of local exhaust devices mounted on an articulated extract arm by measuring the possible positions of the opening of the device;
- a method for measuring the pressure drop and noise level in the type test;
- instructions for marking the device and recommended content of information for use;
- guidance for use describing the limitations of local exhaust devices with articulated extract arm for different airflow rates establishing the capture zone;
- guidance on selection, installation, commissioning, and control testing of articulated extract arms and their local exhaust ventilation systems.
The scope does not include filtration requirements and impact of fully or partly recirculation of the airflow extracted by an articulated extract arm.

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The scope of the Amendment is the same as EN 61010-2-101:2017. It applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.

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This standard EN 61010-2-101:2017 Safety requirements for electrical equipment for measurement, control and laboratory use is classified in these ICS categories:
19.080 Electrical and electronic testing
71.040.10 Chemical laboratories. Laboratory equipment
11.040.55 Diagnostic equipment
IEC 61010-2-101:2015 is available as IEC 61010-2-101:2015 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.
IEC 61010-2-101:2015 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety function, as specified in IEC Guide 104. This standard has been prepared in close collaboration with Working Group CENELEC BTTF 88.1. This second edition cancels and replaces the first edition published in 2002. It constitutes a technical revision and includes the following significant changes from the first edition, as well as numerous other changes:
- excluded IEC 61010-2-081 (general laboratory equipment) from the scope. This separates IEC 61010-2-081 and IEC 61010-2-101 equipment;
- updated Biohazard and Lot symbols in Table 1 in Clause 5;
- added requirement for within expiration consumables and authorized representative details in Instructions for Use to Clause 5;
- added requirement for gas or liquid markings and ratings to Clause 5;
- added requirement to include OPERATOR instructions to deal with consumable or sample spills, jams or breakage inside equipment, disposal of hazardous waste, personal protection, RISK reduction procedures relating to flammable liquids, burns from surfaces, and loading and unloading of sample and reagents in Instructions for Use to Clause 5;
- added requirement for manufacturer to provide instructions on equipment transport, storage and removal from use to Clause 5;
- added normative reference ISO 18113-5 for instructions for use of self-test IVD medical equipment in Clause 5;
- added requirement for OPERATOR maintenance instructions to Clause 7;
- added requirements for sample zones and loading zones to Clause 7;
- excluded equipment whose size and weight make unintentional movement unlikely from drop test in Clause 8;
- added requirement for biohazard marking to Clause 13;
- added requirement for interlock systems containing electric/electronic or programmable components to Clause 15;
- added informative reference to Usability standard IEC 62366 to Clause 16;
- replaced Clause 17 with requirements of ISO 14971 for RISK assessment.
- Annex BB Instructions for use for self-testing IVD Medical Equipment deleted and a reference given to ISO 18113-5 in Clause 5.

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This document specifies
—    metrological requirements,
—    maximum permissible errors,
—    requirements for marking and
—    information to be provided for users,
for air-displacement (type A) and positive displacement (type D) single-channel and multi-channel pipettes, complete with their selected tip(s) and any other essential, consumable parts, designed to deliver the selected volume (Ex).

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This document specifies
—    metrological requirements,
—    maximum permissible errors,
—    requirements for marking and
—    information to be provided for users,
for dispensers. It is applicable to dispensers with nominal volumes from 1 μl up to 200 ml, designed to deliver their volume (Ex).

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This document specifies general requirements for piston-operated volumetric apparatus (POVA). It is applicable to pipettes, burettes, dilutors, dispensers and manually operated precision laboratory syringes. It furthermore defines terms for the use of piston-operated volumetric apparatus and gives user recommendations.
This document does not apply to medical products intended for use on humans, e.g. for medical syringes.

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This document specifies
—    metrological requirements,
—    maximum permissible errors,
—    requirements for marking and
—    information to be provided for users,
for manually operated precision laboratory syringes made of glass or glass and metal designed to deliver their selected volume (Ex).
Manually operated precision laboratory syringes are instruments used for delivering liquids and gases. The barrel is typically made of glass and the plunger and the needle are typically made of metal.

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This document specifies a gravimetric reference measurement procedure for the determination of volume of piston-operated volumetric apparatus (POVA). The procedure is applicable to complete systems comprising the basic apparatus and all parts selected for use with the apparatus, disposable or reusable, involved in the measurement by delivery (Ex) or contained (In).

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This document specifies alternative measurement procedures for the determination of  volume of piston-operated volumetric apparatus.
The procedures are applicable to complete systems comprising the basic apparatus and all parts selected for use with the apparatus, disposable or reusable, involved in the measurement by delivery process (Ex). Methods described in this document are suitable for various maximum nominal volumes of piston-operated volumetric apparatus. It is the responsibility of the user to select the appropriate method.

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This document specifies
—    metrological requirements,
—    maximum permissible errors,
—    requirements for marking and
—    information to be provided for users,
for dilutors with a sample uptake capacity (In) from 5 μl to 1 ml and a diluent capacity (Ex) from 50 μl to 100 ml. They are designed to deliver the sample and diluent together in measured proportion and measured volume.

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This document specifies
—    metrological requirements,
—    maximum permissible errors,
—    requirements for marking and
—    information to be provided for users,
for burettes. This document is applicable to burettes with nominal volumes up to 100 ml, designed to deliver their specified volume (Ex).

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This document specifies the photometric reference measurement procedure for the determination of volume of piston-operated volumetric apparatus (POVA). The procedure is applicable to complete systems comprising the basic apparatus with a maximum nominal volume of 5 000 µl and all parts selected for use with the apparatus, disposable or reusable, involved in the measurement by delivery (Ex).

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This document gives guidance and requirements on the optimization of sputter-depth profiling parameters using appropriate single-layered and multilayered reference materials, in order to achieve optimum depth resolution as a function of instrument settings in Auger electron spectroscopy, X-ray photoelectron spectroscopy and secondary ion mass spectrometry. This document is not intended to cover the use of special multilayered systems such as delta doped layers.

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This part of the standard specifies a test method (using liquid chromatography, LC) for detection and quantification of all extractable neutral, ionic, perfluorinated and polyfluorinated non-volatile substances in textile products (for example, in fabrics treated with fluorochemical finishes and in coated fabrics).
Classes of volatile and non volatile compounds (regulated and of concern) in Table 1 include acids, salt acids, esters, amides, telomers, sulfonates, sulfonamides and sulfonamidalcohols.

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This part of the standard specifies a test method (using gas chromatography, GC) for detection and
quantification of al l extractable perfluorinated and polyfluorinated v ol at i le substances in textile
products (for example, in fabrics treated with fluoro-chemical finishes and in coated fabrics).
Classes of volatile and non volatile (Part 1 of this Standard) compounds (regulated and of
concern) in Table 1 include acids, salt acids, esters, amides, telomers, sulfonates, sulfonamides and
sulfonamidalcohols.

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This document specifies requirements and recommendations for organizations directly or indirectly involved in the cannabis supply chain, to enable them to: — plan, implement, operate, maintain and update a good production practice programme for providing products that are safe, according to their intended use; — demonstrate compliance with applicable statutory and regulatory requirements; — evaluate and assess mutually agreed customer requirements and demonstrate conformity to them; — effectively communicate with interested parties and demonstrate conformity to relevant interested parties; — demonstrate conformity to stated policies in a cannabis quality programme (CQP) for product safety, product quality, product security and facility safety; — support the evaluation of quality programmes by external organizations or to permit self-assessment or self-declaration of adherence to some or all of the guidance contained in this document. All requirements in this document are generic and intended to be applicable to all organizations in the cannabis supply chain, regardless of size and/or complexity. Organizations that are directly or indirectly involved include (but are not limited to) growers/cultivators, harvesters, primary processors, producers of cannabis, manufacturers of cannabis derivatives, cannabis edibles and/or cannabis products, testing providers, retailers and organizations providing transportation, storage and distribution services, suppliers of equipment, packaging materials and other contact materials. This document intended to enable any organization, including small and/or less developed organizations, to implement externally developed elements in its CQP. NOTE 1 Organizations in the cannabis supply chain are diverse in nature and not all the requirements specified in this document apply to each establishment or process. Justifications for exclusions or the use of alternative measures can be documented by a risk assessment/hazard analysis or other appropriate means. This document provides guidance related to the following categories of cannabis, cannabis derivatives and cannabis products: — cannabis plant seeds; — cannabis plants; — fresh cannabis; — dried cannabis; — cannabis derivatives; — cannabis topicals; — inhalable cannabis. NOTE 2 Annex B provides additional guidance on applying GPP to cannabis edibles with respect to requirements and recommendations in existing food safety standards. Where buildings or premises combine cultivation and processing of cannabis plants, including ancillary activities, along with other operational activities, the requirements and recommendations in this document apply only to that portion of the facility. NOTE 3 Where joint use activities are present in a common building, specific statutory and regulatory requirements can apply for each category. This document does not address the following: — requirements related to research and development activities for finished products; — general fire prevention or building construction features that are normally a function of local building and fire codes where applicable; — premises used exclusively for operational activities, such as office space, call centres and retail outlets, used for the distribution, marketing, or sale of cannabis; NOTE 4 Shipping and receiving of products from the production facility for further distribution are not considered as a retail outlet. — the safe consumption or use of the cannabis or cannabis products produced by organizations applying these good production practices; — occupational health and safety requirements governing cannabis workers and personnel except as identified in A.8.4 and A.8.6; — the protection of the environment; — security of the supply chain monitoring system, including cybersecurity and notifications; NOTE 5 Security and monitoring of the supply chain are dealt with specifically in IWA 37-2. — outdoor cultivation of cannabis and industrial hemp; — gr

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This document presents a simple format for the exchange of digital spectral data that has been designated as an EMSA/MAS standard. This format is readable by both humans and computers and is suitable for transmission through various electronic networks, the phone system (with modems) or on physical computer storage devices (such as removable media). The format is not tied to any one computer, programming language or computer operating system. The adoption of a standard format enables different laboratories to freely exchange spectral data, and helps to standardize data analysis software. If equipment manufacturers were to support a common format, the microscopy and microanalysis community would avoid duplicated effort in writing data analysis software.

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This document specifies a glow discharge optical emission spectrometric method for the determination of the thickness and mass per unit area of single and metallic nanolayers on iron-based substrates. This method is applicable to single and metallic nanolayers, 10 nm to 100 nm thick, on iron-based substrates. The metallic elements of the layers are Cr, Ni, Ti, Mn and Al. Other elements that can be determined according to this document are P and S.

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This document specifies a method for determining the maximum count rate for an acceptable limit of divergence from linearity of the intensity scale in single ion counting time-of-flight (TOF) secondary ion mass spectrometers using a test based on isotopic ratios in spectra from poly(tetrafluoroethylene) (PTFE). It also includes a method to correct for intensity nonlinearity arising from intensity lost from a microchannel plate (MCP) or scintillator and photomultiplier followed by a time-to-digital converter (TDC) detection system caused by secondary ions arriving during its dead-time. The correction can increase the intensity range for 95 % linearity by a factor of up to more than 50 so that a higher maximum count rate can be employed for those spectrometers for which the relevant correction formulae have been shown to be valid.

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This document specifies performance requirements and test methods for remote alcohol monitoring devices that use breath alcohol testing technology. It covers remote alcohol monitoring devices having a mouthpiece and which are intended to be used by participants in programmes designed to monitor alcohol consumption. This document is directed at test laboratories and manufacturers of remote alcohol monitoring devices. It defines requirements and test procedures for type testing. Several parameter settings (such as alcohol concentration, breath volume or units of measurement) are specified in this document for the purpose of type testing according to this standard only. However, it may be necessary due to national regulations or depending on user requests to set the values of the prescribed parameter settings differently when the remote alcohol monitoring devices are in use.

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This document specifies a test method for the determination of the content of mono-aromatic, di-aromatic and tri+-aromatic hydrocarbons in diesel fuels, paraffinic diesel fuels and petroleum distillates.
This document defines two procedures, A and B.
Procedure A is applicable to diesel fuels that may contain fatty acid methyl esters (FAME) up to 30 % (V/V) (as in [1], [2] or [3]) and petroleum distillates in the boiling range from 150 °C to 400 °C (as in [4].
Procedure B is applicable to paraffinic diesel fuels with up to 7 % (V/V) FAME. This procedure does not contain a dilution of the sample in order to determine the low levels of aromatic components in these fuels.
The polycyclic aromatic hydrocarbons content is calculated from the sum of di-aromatic and tri+-aromatic hydrocarbons and the total content of aromatic compounds is calculated from the sum of the individual aromatic hydrocarbon types.
Compounds containing sulfur, nitrogen and oxygen can interfere in the determination; mono-alkenes do not interfere, but conjugated di-alkenes and poly-alkenes, if present, can do so.
NOTE 1   For the purpose of this European Standard, the terms "% (m/m)" and "% (V/V)" are used to represent the mass fraction, µ, and the volume fraction, φ, of a material respectively.
NOTE 2   By convention, the aromatic hydrocarbon types are defined on the basis of their elution characteristics from the specified liquid chromatography column relative to model aromatic compounds. Their quantification is performed using an external calibration with a single aromatic compound for each of them, which may or may not be representative of the aromatics present in the sample. Alternative techniques and test methods may classify and quantify individual aromatic hydrocarbon types differently.
NOTE 3   Backflush is part of laboratory-internal maintenance.
WARNING - The use of this standard can involve hazardous materials, operations and equipment. This standard does not purport to address all of the safety problems associated with its use. It is the responsibility of users of this standard to take appropriate measures to ensure the safety and health of personnel prior to application of the standard, and fulfil statutory and regulatory requirements for this purpose.

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This document specifies an analytical method to quantify nicotine of collected vapour product
emissions by gas chromatography.

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This document defines terms relating to automated liquid handling systems (ALHS). This document also specifies general requirements for the use of ALHS. It describes types of ALHS and specific use requirements, settings, and adjustments for each ALHS type. It also specifies environmental requirements for the use of ALHS. This document is applicable to all ALHS with complete, installed liquid handling devices, including tips and other essential parts needed for delivering a specified volume, which perform liquid handling tasks without human intervention into labware. NOTE Measurement procedures for the determination of volumetric performance are given in ISO 23783-2. The determination, specification, and reporting of volumetric performance of automated liquid handling systems are described in ISO 23783-3.

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This document specifies procedures for the determination of volumetric performance of automated liquid handling systems (ALHS), including traceability and estimations of measurement uncertainty of measurement results. This document is applicable to all ALHS with complete, installed liquid handling devices, including tips and other essential parts needed for delivering a specified volume, which perform liquid handling tasks without human intervention into labware. NOTE For terminology and general requirements of automated liquid handling systems, see ISO 23783-1. Determination, specification, and reporting of volumetric performance of automated liquid handling systems is described in ISO 23783-3.

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This document provides guidance and establishes requirements for collecting and examining volumetric performance data of automated liquid handling systems (ALHS). It specifies how to index and track volumetric performance data and provides descriptive statistics for the evaluation of these data. This document also specifies reporting requirements of ALHS volumetric performance. This document is applicable to all ALHS with complete, installed liquid handling devices, including tips and other essential parts needed for delivering a specified volume, which perform liquid handling tasks without human intervention into labware. NOTE For terminology and general requirements of automated liquid handling systems, see ISO 23783-1. Measurement procedures for the determination of volumetric performance are given in ISO 23783-2.

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IEC 61207-3:2019 is available as IEC 61207-3:2019 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition. IEC 61207-3:2019 applies to the three main methods for measuring oxygen by its paramagnetic property, which are outlined in the introduction. It considers essential ancillary units and applies to analyzers installed indoors and outdoors. Safety-critical applications can require additional requirements from system and analyzer specifications not covered in this document. This document is intended: - to specify terminology and definitions related to the functional performance of paramagnetic gas analyzers for the measurement of oxygen in a source gas; - to unify methods used in making and verifying statements on the functional performance of such analyzers; - to specify what tests are performed to determine the functional performance and how such tests are carried out; - to provide basic documents to support the application of internationally recognized quality management standards. This third edition cancels and replaces the second edition published in 2002. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition: a) all references (normative and informative) have been updated, deleted or added to as appropriate; b) all the terms, descriptions and definitions relating to the document have been updated where appropriate; c) all references to “errors” have been replaced by “uncertainties” and appropriate updated definitions applied.

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Applies to gas analyzers using high temperature electrochemical sensors for measurement of oxygen in gas. Applies to both 'in situ' and extractive analyzers installed indoors or outdoors.

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This document specifies the interface between an alcohol interlock for production and aftermarket installation and a vehicle. It details the modes of electrical connections, the assignment of electrical connection lines as well as the information to be exchanged between the vehicle and the alcohol interlock. This document is applicable to alcohol interlocks for drink-driving-offender programmes (as in EN 50436 1) as well as to alcohol interlocks for general preventive use (as in EN 50436 2). This document is mainly directed at manufacturers of alcohol interlocks and at vehicle manufacturers. This document is referenced in EN 50436 7 and provides details of the preferred data bus connection suggested therein. NOTE This document describes the information exchange using a LIN or a CAN (J1939) connection.

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