Pregled nacrta

ISO 15136-1:2009 provides requirements for the design, design verification and validation, manufacturing and data control, performance ratings, functional evaluation, repair, handling and storage of progressing cavity pumps for use in the petroleum and natural gas industry. ISO 15136-1:2009 is applicable to those products meeting the definition of progressing cavity pumps (PCP) included herein.
Connections to the drive string and tubulars are not covered in ISO 15136-1:2009.
ISO 15136-1:2009 establishes requirements for characterization and testing of stator elastomer material, design validation and functional evaluation and provides information for PCP elastomer selection and testing, installation, start-up and operation guidelines, equipment selection and application guidelines, functional specification form, used pump evaluation, drive string selection and use, repair and reconditioning procedures and auxiliary equipment.
Equipment not covered by the requirements of ISO 15136-1:2009 includes bottom-drive systems except for the PCP components, drive-string components and auxiliary equipment such as tag bars, gas separators and torque anchors.

This document applies to medical devices other than in vitro diagnostic medical devices manufactured utilizing materials of human origin. The materials are non-viable or have been rendered non-viable. The document specifies, in junction with ISO 14971, a procedure to identify the hazards and hazardous situations associated with such devices, to estimate and evaluate the resulting risks, to control these risks and to monitor the effectiveness of that control.  Furthermore, it outlines the decision process for the residual risk acceptability, taking into account the balance of residual risk, as defined in ISO 14971, and expected medical benefit as compared to available alternatives. This document is intended to provide requirements and guidance on risk management related to the hazards typical of medical devices manufactured utilizing human tissues or derivatives such as: 

a) contamination by bacteria, moulds or yeasts; 
b) contamination by viruses; 
c) contamination by agents causing Transmissible Spongiform Encephalopathies (TSE); 
d) material responsible for undesired pyrogenic, immunological or toxicological reactions. 

For parasites and other unclassified pathogenic entities, similar principles can apply. 
This document does not stipulate levels of acceptability, because they are determined by a multiplicity of factors. 
This document does not specify a quality management system for the control of all stages of production of medical devices.

This document specifies a common method for the quantitative chemical analysis of various mixtures of fibres. This method and the methods described in the other parts of ISO 1833 are applicable, in general, to fibres in any textile form. Where certain textile forms are excepted, these are listed in the scope of the appropriate part.

This document specifies the characteristics, test methods, qualification and acceptance conditions of single and multicore electric cables, without jackets, for general purpose with conductors in copper or copper alloy, intended for installation in aircraft circuits.

The insulation of these cables is designed to withstand aircraft voltages at a frequency not exceeding 2 000 Hz. Unless specified by individual product standards the maximum demonstrated A.C. voltage of rating of these cables is 115 V RMS (phase to neutral) and 200 V RMS (phase to phase).

They are divided into types, the characteristics of which are given in the product standards. Unless otherwise specified in the product standard, the tests defined in this document apply.

This document specifies requirements and recommendations that can enable an organization to design, develop and provide products and services so that they can be accessed, understood and used by the widest range of users, including persons with disabilities.
This document specifies requirements and recommendations that can enable an organization to widen their range of users by identifying diverse needs, characteristics, capabilities, and preferences, by directly or indirectly involving users, and by using knowledge about accessibility in its procedures and processes.
This document specifies requirements that can enable an organization to meet applicable statutory and regulatory requirements as related to the accessibility of its products and services.
The requirements and recommendations set out in this document are generic and are intended to be applicable to all relevant parts of all organisations, regardless of type, size or products and services provided.
This document promotes accessibility following a Design for All approach in mainstream products and services and interoperability of these with assistive technologies.

This document provides a systematized framework for the competencies of AI ethicists, categorizing them into knowledge, skills and attitudes related to the specific activities and tasks of the role. It identifies requirements and recommendations necessary for individuals to effectively perform as AI ethicists. These competencies encompass a strong understanding of European values and fundamental rights, further enhancing the knowledge, skills and attitudes required for this profession.
The document aims to foster a shared understanding of the essential concepts and principles inherent to the AI ethicist role. It illustrates a clear, uniform approach to the integral components of this profession.
Moreover, the document outlines how the role of AI ethicists can be seamlessly integrated into a wide variety of organizations. These include, but are not limited to, commercial enterprises, governmental agencies and non-profit organizations.

ISO 11615:2017 establishes definitions and concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products.
Taken together, the standards listed in the Introduction define, characterise and uniquely identify regulated Medicinal Products for human use during their entire life cycle, i.e. from development to authorisation, post-marketing and renewal or withdrawal from the market, where applicable.
Furthermore, to support successful information exchange in relation to the unique identification and characterisation of Medicinal Products, the use of other normative IDMP messaging standards is included, which are to be applied in the context of ISO 11615:2017.

ISO 15614-1:2017 specifies how a preliminary welding procedure specification is qualified by welding procedure tests.
ISO 15614-1:2017 applies to production welding, repair welding and build-up welding.
ISO 15614-1:2017 defines the conditions for the execution of welding procedure tests and the range of qualification for welding procedures for all practical welding operations within the qualification of this document.
The primary purpose of welding procedure qualification is to demonstrate that the joining process proposed for construction is capable of producing joints having the required mechanical properties for the intended application.
Two levels of welding procedure tests are given in order to permit application to a wide range of welded fabrication. They are designated by levels 1 and 2. In level 2, the extent of testing is greater and the ranges of qualification are more restrictive than in level 1.
Procedure tests carried out to level 2 automatically qualify for level 1 requirements, but not vice-versa.
When no level is specified in a contract or application standard, all the requirements of level 2 apply.
This document applies to the arc and gas welding of steels in all product forms and the arc welding of nickel and nickel alloys in all product forms.
Arc and gas welding are covered by the following processes in accordance with ISO 4063.
111 - manual metal arc welding (metal-arc welding with covered electrode);
114 - self-shielded tubular-cored arc welding;
12 - submerged arc welding;
13 - gas-shielded metal arc welding;
14 - gas-shielded arc welding with non-consumable electrode;
15 - plasma arc welding;
311 - oxy-acetylene welding.
The principles of this document may be applied to other fusion welding processes.
NOTE A former process number does not require a new qualification test according to this document.
Specification and qualification of welding procedures that were made in accordance with previous editions of this document may be used for any application for which the current edition is specified. In this case, the ranges of qualification of previous editions remain applicable.
It is also possible to create a new WPQR (welding procedure qualification record) range of qualification according to this edition based on the existing qualified WPQR, provided the technical intent of the testing requirements of this document has been satisfied. Where additional tests have to be carried out to make the qualification technically equivalent, it is only necessary to perform the additional test on a test piece.

This document specifies requirements for classification of covered electrodes and deposited metal in the as-welded condition and in the post-weld heat-treated condition for manual metal arc welding of high-strength steels with a minimum yield strength greater than 500 MPa or a minimum tensile strength greater than 570 MPa.
This document is a combined specification providing a classification utilizing a system based on the yield strength and an average impact energy of 47 J of the all-weld metal, or utilizing a system based on the tensile strength and an average impact energy of 27 J of the all-weld metal.
a) Subclauses and tables which carry the suffix letter "A" are applicable only to covered electrodes classified under the system based on the yield strength and an average impact energy of 47 J of the all-weld metal given in this document.
b) Subclauses and tables which carry the suffix letter "B" are applicable only to covered electrodes classified under the system based on the tensile strength and an average impact energy of 27 J of the all-weld metal given in this document.
c) Subclauses and tables which do not have either the suffix letter "A" or the suffix letter "B" are applicable to all covered electrodes classified under this document.

This document contains general requirements and measures for machinery that performs packaging functions for: 
— Conditioning of products and packaging materials 
— Primary (first) packaging, secondary (second) packaging and tertiary (third) packaging.

This document provides guidelines for selecting the measuring device, measuring geometry and temperature control unit. The general principles of test performance are described, and example evaluations of rotational and oscillatory rheometry are provided.

This document specifies test methods for the determination of the resistance of footwear against selected chemicals for the following circumstances: splashing, degradation, and permeation.

This document specifies requirements for footwear to protect the user against limited contact in time with specific chemicals.
The following risks are covered: splashing and degradation by chemical.

This document specifies requirements for footwear intended to protect the wearer from a prolonged continuous contact (more than 1 hour) with specific chemicals.
Degradation and permeation by chemicals are addressed in this document. Other requirements are covered by reference to EN ISO 20345:2022+A1:2024, EN ISO 20346+A1:2024:2022 or EN ISO 20347:2022+A1:2024 as appropriate.

This document complements the core rules for the product category of construction products as defined in EN 15804:2012+A2:2019 and is intended to be used as a c-PCR in conjunction with that standard.
This c-PCR applies to products within the scope of CEN/TC 166, i.e. to products for chimneys,
- which are flue liners with sections and, fittings, and where appropriate insulation, additional walls, outer walls, air supply ducts, terminals and other components which include a new category named as accessories;
- with flue liners manufactured from metal, clay/ceramics, concrete or plastic.
Chimneys are system chimneys, connecting flue pipes or custom-built chimneys.
This document defines the parameters to be reported, what EPD types (and life cycle stages) to be covered, what rules to be followed in order to generate Life Cycle Inventories (LCI) and conduct Life Cycle Impact Assessment (LCIA) and the data quality to be used in the development of EPDs.
NOTE The assessment of social and economic performances at product level is not covered by this document.

This document specifies the additional technical delivery conditions for castings made from all cast iron materials.
This document applies to iron castings produced in sand or permanent moulds or by centrifugal casting, continuous casting or investment casting.

This part of EN 455 specifies requirements for the evaluation of biological safety for medical gloves for single use. It gives requirements for labelling and the disclosure of information relevant to the test methods used.