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ISO 14025:2006 establishes the principles and specifies the procedures for developing Type III environmental declaration programmes and Type III environmental declarations. It specifically establishes the use of the ISO 14040 series of standards in the development of Type III environmental declaration programmes and Type III environmental declarations.
ISO 14025:2006 establishes principles for the use of environmental information, in addition to those given in ISO 14020:2000
Type III environmental declarations as described in ISO 14025:2006 are primarily intended for use in business-to-business communication, but their use in business-to-consumer communication under certain conditions is not precluded.

This document specifies the technical requirements of rectangular connectors with sealed and non-sealed rear, plastic housing, locking device, for operating temperatures from -55 °C to 175 °C.

This document specifies the requirements relating to:
Steel GX5CrNiCuNb16-4 (1.4525)
Homogenized
Solution treated and precipitation hardened
Investment casting
De ≤ 50 mm
Rm ≥ 900 MPa
for aerospace applications.

This document defines basic terms, symbols, and units of measurement for the field of laser technology in order to unify the terminology and to arrive at clear definitions and reproducible tests of beam parameters and laser-oriented product properties.
NOTE The laser hierarchical vocabulary laid down in this document differs from that given in IEC 60825?1. ISO and IEC have discussed this difference and agree that it reflects the different purposes for which the two standards serve. For more details, see informative Annex A.

This document specifies the requirements and test procedures for 360° visibility of self-propelled industrial rider-controlled pallet-stacking trucks in accordance with ISO 5053-1 (herein after referred to as trucks), without a load and it is intended to be used in conjunction with EN 16842-1.
This document also applies to pedestrian controlled trucks with foldable platform when used in ride-on mode.
Pedestrian-controlled and pedestrian-propelled trucks are not covered by this document.
Where specific requirements in this part are modified from the general requirements in EN 16842-1, the requirements of this part are truck specific and intended to be used for self-propelled industrial stand-on pallet-stacking trucks.
This part of EN 16842 deals with all significant hazards, hazardous situations or hazardous events relevant to the visibility of the operator for applicable machines when used as intended and under conditions of misuse which are reasonably foreseeable by the manufacturer.

This European Standard specifies requirements for chemical and physical properties, and minimum performance requirements of medium expansion foams suitable for surface application to water-immiscible liquids. Requirements are also given for marking.
WARNING - Any type approval according to this standard is invalidated by any change in composition of the approved product.
Some concentrates conforming to this part of EN 1568 can also conform to other parts and therefore can also be suitable for application as low and/or high expansion foams.

This European Standard specifies requirements for chemical and physical properties, and minimum performance requirements of high expansion foams suitable for surface application to water-immiscible liquids. Requirements are also given for marking.
WARNING - Any type approval according to this standard is invalidated by any change in composition of the approved product.
Some concentrates conforming to this part of EN 1568 can also conform to other parts and therefore can also be suitable for application as low and/or medium expansion foams.

This European Standard specifies requirements for chemical and physical properties, and minimum performance requirements of low expansion foams suitable for surface application to water-immiscible liquids. Requirements are also given for marking.
WARNING - Any type approval according to this standard is invalidated by any change in composition of the approved product.
Some concentrates conforming to this part of EN 1568 can also conform to other parts and therefore can also be suitable for application as medium and/or high expansion foams, and for application at low expansion to water-miscible liquids.

This document provides guidelines for the design, construction, use and maintenance of hardened protective shelters (further referred to in this standard as “shelters”). It offers guidance related to the parts, features, equipment, actions and responsibilities related to each phase of the life cycle of a shelter.

This document is intended for organizations or individuals being responsible for or involved in decision-making, planning, implementation, administration, use or upkeep of shelters, such as local, regional and national governments, civil protection agencies, first responders and businesses such as designers, constructers and equipment suppliers.

This document does not cover the minimum requirements or exact specifications for the properties of or actions related to a shelter, as these normally are detailed in national legislation and regulations of each country; nor does it cover rapidly erected temporary shelters, such as lightweight canvas weather shelters, other tarp tent shelters, or metal and container shelters.

This document specifies the control and approval of in vitro diagnostic reagents used in animal health for the detection, and/or absolute quantification of pathogen-specific nucleic acid (DNA or RNA) by PCR (e.g. endpoint PCR, real-time PCR, reverse transcription-PCR).
This document is applicable to diagnostic reagents as a priority for infectious diseases (due to bacteria, viruses, fungi, or parasites, including genetic markers associated with pathogenicity, such as antimicrobial resistance or toxin production) and associated animal species for which harmonization of practices in this area is needed, i.e. those for which the national, regional or international regulatory framework provides for the control of trade in animals and/or animal products and/or the definition of a health status (absence of infection) of areas, establishments or individuals. Anyhow, all reagents designated by the competent authorities fall under the scope of this document. Nevertheless, the authorities or any other animal health stakeholder can choose to derogate in specific and very limited situations such as emerging, exotic or rare diseases.
This document is not applicable to all existing diagnostic reagents, in particular those for which certain parameters described in this document cannot be validly evaluated in accordance with international requirements, due, e.g. to the absence of a specific reference standard and/or accessible and duly validated reference materials.
The PCR diagnosis usually involves the use of a nucleic acid extraction and/or purification reagent, and a PCR reagent. The PCR method (when applicable) involves the successive use of these distinct reagents. PCR reagent control can be performed if the applicant provides evidence of the validity of the PCR reagent for use in the animal health diagnostic analysis, by proving its diagnostic performances with nucleic acid extracts obtained from the different matrices described in the instruction for use. The control of a complete PCR method by the applicant and the control organization is performed only if the PCR reagent cannot be dissociated from an nucleic acid extraction and/or purification systems. This document does not cover the control of the nucleic acid extraction and/or purification reagents, only.
This document does not cover the step in which the user verifies a reagent (analysis method adoption).
NOTE   Prion diseases are not included in the scope of this third part of the EN 18000 series. Unlike other infectious diseases, prion diseases are not diagnosed using PCR assays because prions lack a nucleic acid component and consist solely of an abnormally folded conformer of the normal host protein.

ISO 14025:2006 establishes the principles and specifies the procedures for developing Type III environmental declaration programmes and Type III environmental declarations. It specifically establishes the use of the ISO 14040 series of standards in the development of Type III environmental declaration programmes and Type III environmental declarations.
ISO 14025:2006 establishes principles for the use of environmental information, in addition to those given in ISO 14020:2000
Type III environmental declarations as described in ISO 14025:2006 are primarily intended for use in business-to-business communication, but their use in business-to-consumer communication under certain conditions is not precluded.

ISO 10993-3:2014 specifies strategies for risk estimation and selection of hazard identification tests, with respect to the possibility of the following potentially irreversible biological effects arising as a result of exposure to medical devices:

genotoxicity;
carcinogenicity;
reproductive and developmental toxicity.

ISO 10993-3:2014 is applicable when the need to evaluate a medical device for potential genotoxicity, carcinogenicity, or reproductive toxicity has been established.

ISO 10993-3:2014 specifies strategies for risk estimation and selection of hazard identification tests, with respect to the possibility of the following potentially irreversible biological effects arising as a result of exposure to medical devices:

genotoxicity;
carcinogenicity;
reproductive and developmental toxicity.

ISO 10993-3:2014 is applicable when the need to evaluate a medical device for potential genotoxicity, carcinogenicity, or reproductive toxicity has been established.

ISO 22032:2006 specifies a method for the determination of selected polybrominated diphenyl ethers (PBDE) in sediment and sludge using gas chromatography/mass spectrometry (GC-MS) in the electron impact (EI) or negative ion chemical ionization (NCI) mode. 
When using GC-EI-MS, the method is applicable to samples containing 0,05 to 25 micrograms per kilogram of tetra- to octabromo congeners and 0,3 to 100 micrograms per kilogram of decabromo diphenyl ether (BDE-209), respectively.

ISO 4259-2:2017 specifies the methodology for the application of precision estimates of a test method derived from ISO 4259‑1. In particular, it defines the procedures for setting the property specification limits based upon test method precision where the property is determined using a specific test method, and in determining the specification conformance status when there are conflicting results between supplier and receiver. Other applications of this test method precision are briefly described in principle without the associated procedures.
The procedures in ISO 4259-2:2017 have been designed specifically for petroleum and petroleum-related products, which are normally homogeneous. However, the procedures described in ISO 4259-2:2017 can also be applied to other types of homogeneous products. Careful investigations are necessary before applying ISO 4259-2:2017 to products for which the assumption of homogeneity can be questioned.

ISO 18739:2016 specifies terms, synonyms for terms and definitions used in the process chain for CAD/CAM systems in dentistry.