There are no changes to the content of the EN 14375 document.
This document specifies performance requirements and methods of test for non-reclosable packaging that have been designated child-resistant. This document is intended for type approval only (see 3.5) and is not intended for quality assurance purposes.

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There are no changes to the content of the EN 862 document apart from the addition of Clause 2, Normative references.
This document specifies performance requirements and methods of test for non-reclosable packaging that has been designated child-resistant and which is intended to contain non-pharmaceutical products. This document is intended for type approval only (see 2.5) and is not intended for quality assurance purposes.
This document applies to non-reclosable packages of the single-use type consisting of one or more individual units.
Non-reclosable packages for pharmaceutical products are excluded from the scope of this document. These are the subject of a separate standard, ISO 14375, Child-resistant non-reclosable packaging for pharmaceutical products — Requirements and testing.

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This document specifies performance requirements and methods of test for non-reclosable packaging that have been designated child-resistant. This document is intended for type approval only (see 3.5) and is not intended for quality assurance purposes.

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This document specifies performance requirements and methods of test for non-reclosable packaging that has been designated child-resistant and which is intended to contain non-pharmaceutical products. This document is intended for type approval only (see 2.5) and is not intended for quality assurance purposes.
This document applies to non-reclosable packages of the single-use type consisting of one or more individual units.
Non-reclosable packages for pharmaceutical products are excluded from the scope of this document. These are the subject of a separate standard, ISO 14375, Child-resistant non-reclosable packaging for pharmaceutical products — Requirements and testing.

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This document describes the general specifications of temperature-sensitive medicinal packaging based on the principles of good distribution practice (GDP). It also specifies test methods to validate the package performance for temperature-sensitive medicinal products. This covers the procedures of temperature-recording and testing methods on the performance of insulated containers such as dimensions, weights, storage capacity and robustness in temperature-controlling. This document does not guarantee the quality and safety of all medicinal products. Under special circumstances where the weight or the characteristics of the products and environment show specific conditions, agreements are followed. This document does not cover the active packaging system, but only covers the passive packaging system able to control the desired temperature without any power sources.

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This document lists the relevant standards from various fields and provides a standardization roadmap for hyperloop systems. The roadmap will provide guidance on the applicable standards from various fields, those that need amending and the new-to be developed standards.

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This document lists the relevant standards from various fields and provides a standardization roadmap for hyperloop systems. The roadmap will provide guidance on the applicable standards from various fields, those that need amending and the new-to be developed standards.

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IEC 60286-2:2022 applies to the tape packaging of components with two or more unidirectional leads for use in electronic equipment. It provides dimensions and tolerances necessary to tape components with unidirectional leads. In general, the tape is applied to the component leads.
It covers requirements for taping techniques used with equipment for automatic handling, pre-forming of leads, insertion and other operations and includes only those dimensions which are essential to the taping of components intended for the above-mentioned purposes.
This edition includes the following significant technical changes with respect to the previous edition:
a) complete revision of structure;
b) consolidation of essential parameters and requirements in Clause 4.

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This document specifies the information needed for the design type testing of packaging, intermediate bulk containers (IBCs) and large packaging intended for use in the transport of dangerous goods.
NOTE 1   This document can be used in conjunction with one or more of the international regulations set out in the Bibliography.
NOTE 2   The term “packaging” includes packaging for Class 6.2 infectious substances according to the United Nations.

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This document specifies the information needed for the design type testing of packaging, intermediate
bulk containers (IBCs) and large packaging intended for use in the transport of dangerous goods.
NOTE 1 This document can be used in conjunction with one or more of the international regulations set out in
the Bibliography.
NOTE 2 The term “packaging” includes packaging for Class 6.2 infectious substances according to the United
Nations.

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This document is used in conjunction with and is supplementary to EN 16247-1, Energy audits - Part 1: General requirements. It provides additional requirements to EN 16247-1 and is applied simultaneously.
The procedures described here apply to the different modes of transport (road, rail, marine and aviation), as well as the different ranges (local- to long-distance) and what is transported (i.e. goods and people).
This document specifies the requirements, methodology and deliverables specific to energy audits in the transport sector, every situation in which a displacement is made, no matter who the operator is (a public or private company or whether the operator is exclusively dedicated to transport or not), is also addressed in this document.
This document advises on both the optimization of energy within each mode of transport, as well as selecting the best mode of transport in each situation; the conclusions drawn by the energy audit can influence decisions on infrastructure and investment e.g. in teleconferencing or web meetings.
Energy audits of buildings and processes associated with transport can be conducted respectively with the EN 16247-2 Buildings and EN 16247-3 Processes, e.g. pipelines, depots and escalators/travelators. This part of the standard does not include the infrastructure which supplies energy e.g. the electricity generation of energy for railways.

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This document specifies the information needed for the design type testing of packaging, intermediate bulk containers (IBCs) and large packaging intended for use in the transport of dangerous goods. NOTE 1 This document can be used in conjunction with one or more of the international regulations set out in the Bibliography. NOTE 2 The term “packaging” includes packaging for Class 6.2 infectious substances according to the United Nations.

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This document provides recommended guidelines for the evaluation of colour reproduction capability in the printing of packaging materials. It provides a basis for the development of colour certification schemes by individual brand owners and/or industry associations and for the evaluation of printed results against those schemes.  
Because the package printing supply chain involves multiple partners, both the potential impact of each partner on the overall colour control and the individual responsibilities of each partner are identified in this document. The unique requirements of the individual reproduction processes and their impact on colour reproduction are also identified.

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  • Technical specification
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This document specifies requirements and provides guidance for the application, use and check of tamper verification features to the packaging of medicinal products.

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This document shows some examples of markings (words, numbers or symbols) for the identification of packaging materials. This document is applicable to all types of packaging in order to enable the identification of the materials used.

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This document specifies the test methods of temperature-controlled packages for parcel shipping. Tests include physical, thermal conductivity and insulation performances of transport packages that use insulation for the purpose of blocking thermal conduction between the inside and the outside of a product package that need temperature control.

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This document specifies the general requirements of transport packaging, especially the containers, which are formed or prepared for the temperature-controlled transport services of parcel shipping. Safety or sanitation is not covered in this document. This document set outs the general requirements for transport packaging for safe storage and distribution of temperature-sensitive products.

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This document specifies requirements and provides guidance for the application, use and check of tamper verification features to the packaging of medicinal products.

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This document gives guidance on the application of a quality management system in the manufacture, measuring and monitoring of design type approved dangerous goods packaging, intermediate bulk containers (IBCs) and large packaging.
This document does not include guidance specific to other management systems, such as those for environmental management, occupational health and safety management, or financial management.
It is applicable to an organization that:
a)           needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements; and
b)           aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.
All the guidance in this document is generic and intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.
NOTE       In this document, the terms "product" or "service" only apply to products and services intended for, or required by, a customer.
It does not apply to design type testing, for which reference is made to 6.1.5, 6.3.5, 6.5.6 and 6.6.5 of the UN Model Regulations[27].

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This document specifies requirements for the provision and operation of indirect, temperature-controlled refrigerated delivery services for refrigerated parcels which contain temperature-sensitive goods (including foods) in land transportation. It includes all refrigerated delivery service stages from acceptance (receipt) of a chilled or frozen parcel from the delivery service user to its delivery at the designated destination, including intermediate transfer of the refrigerated parcels between refrigerated vehicles or container and via a geographical routing system. This document also includes requirements for resources, operations and communications to delivery service users. It is intended for application by refrigerated delivery service providers. This document does not cover requirements for: a) refrigerated parcel delivery via modes of transport such as airplane, ship or train; b) refrigerated parcels that are transported in ambient temperatures due to the fact that they contain their own refrigeration materials (for example, ice packs, refrigerated foam bricks, dry ice blocks) and are surrounded and enclosed by sealed thermo protective packaging that creates a separate refrigerated climate to that provided within the delivery service. However, these types of refrigerated parcels may be transported through a refrigerated delivery service; c) direct refrigerated delivery services in which chilled parcels and frozen parcels are collected from the delivery service user and transported directly to a recipient without in-transit transfer; d) the quality or the measurement of the temperature of the contents of the chilled parcels or frozen parcels being delivered and their pre-point of receipt state, however it does set the requirements for the refrigerated delivery service carrying them; e) Medical devices and medical equipment and pharmaceuticals might be subject to specific legislation and require specific transport requirements and are therefore, excluded from the scope of this document. NOTE Resources covered by requirements of this document include facilities, refrigerated vehicles, cold stores, and staff members. This document is not limited to covering specific sizes of vehicles, as long as the performance requirements can be met. Land transport refrigerated vehicles which are conveyed in a ship as roll-on/roll-off vehicles are covered by this document. While this document does not cover requirements directly relating to the quality or safety of the refrigerated parcels being delivered, attention is drawn to specific country legislation that might require a refrigerated delivery service provider to adhere to additional requirements outside of this document, such as monitoring the temperature of the refrigerated parcel itself, or specific requirements regarding the segregation of different types of refrigerated parcel. It is important to note that the contents of refrigerated parcels referenced within this document are not limited to edible or perishable products.

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This document gives guidance on the application of a quality management system in the manufacture, measuring and monitoring of design type approved dangerous goods packaging, intermediate bulk containers (IBCs) and large packaging. This document does not include guidance specific to other management systems, such as those for environmental management, occupational health and safety management, or financial management. It is applicable to an organization that: a) needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements; and b) aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements. All the guidance in this document is generic and intended to be applicable to any organization, regardless of its type or size, or the products and services it provides. NOTE In this document, the terms "product" or "service" only apply to products and services intended for, or required by, a customer. It does not apply to design type testing, for which reference is made to 6.1.5, 6.3.5, 6.5.6 and 6.6.5 of the UN Model Regulations[27].

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This document provides requirements and recommendations in designing consumer packages, independent of material, to increase accessibility with regard to handling and manipulation. The document considers packaging needs from a wide range of users with diverse human abilities and needs in diverse contexts of use. Handling and manipulation include human physical abilities like holding, lifting, carrying, pulling, pushing, sliding, grasping, twisting, tearing and any combination of those actions related to portability, opening, re-closing and taking out contents of packages as well as to storage and disposal. Requirements and recommendations with regard to those abilities are provided for people with special needs including older people and people with disabilities in their handling and manipulation of packages. This document focuses on physical handling and manipulation which necessarily includes the processes of opening and closing specifically detailed in ISO 17480. It applies to reclosable and non-reclosable consumer packaging without using any other mechanical means. This document is primarily for designers, developers and evaluators of packaging and is also useful for other disciplines. Handling and manipulation for transportation of packaging is not covered in this standard. It does not apply to products regulated for safety or other reasons (e.g. toxic or dangerous goods and substances, medicinal products, and medical devices).

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ISO 17480:2015 specifies requirements and recommendations for the accessible design for packaging with a focus on ease of opening. It applies to reclosable and non-reclosable consumer packaging without using any other mechanical means. This International Standard covers the design aspects addressing openability including opening location, opening methods, as well as evaluation techniques, both instrumented and user-based. This International Standard is primarily for designers, developers, and evaluators of packaging and will also be useful for other disciplines.
For products regulated for safety or other reasons (e.g. toxic or dangerous goods and substances, medicinal products, and medical devices), those regulations take precedence.

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This document specifies the methodology and procedure for determining the presence and minimization of other dangerous substances in relation with Annex II Para 1 Indent 3 of Directive 94/62/EC. This document is intended to be of practical use, and to enable efficient application of Directive 94/62/EC, even for small and medium-sized companies in the packaging industry, providing them with a methodology for assessing compliance with the Directive.
This document cannot by itself provide presumption of conformity. The procedure for applying this document is contained in EN 13427.

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This document specifies the methodology and procedure for determining the presence and minimization of other dangerous substances in relation with Annex II Para 1 Indent 3 of Directive 94/62/EC. This document is intended to be of practical use, and to enable efficient application of Directive 94/62/EC, even for small and medium-sized companies in the packaging industry, providing them with a methodology for assessing compliance with the Directive.
This document cannot by itself provide presumption of conformity. The procedure for applying this document is contained in EN 13427.

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This document specifies requirements and provides guidance for the application, use and check of tamper verification features to the packaging of medicinal products.

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ISO 17480:2015 specifies requirements and recommendations for the accessible design for packaging with a focus on ease of opening. It applies to reclosable and non-reclosable consumer packaging without using any other mechanical means. This International Standard covers the design aspects addressing openability including opening location, opening methods, as well as evaluation techniques, both instrumented and user-based. This International Standard is primarily for designers, developers, and evaluators of packaging and will also be useful for other disciplines.
For products regulated for safety or other reasons (e.g. toxic or dangerous goods and substances, medicinal products, and medical devices), those regulations take precedence.

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This document provides general recommendations to be taken into consideration when determining the most suitable type of packaging for products intended for consumers. The functions that packaging can perform include, but are not limited to, containment, protection, handling, transport, storage, convenience, information and presentation. This document also considers the sustainable use of resources covering optimization, reuse and recovery of packaging. This document provides guidance to: — product designers, manufacturers and others engaged in the process of making decisions concerning packaging; — those drafting standards to meet the packaging needs and requirements of consumers as prospective purchasers of products; — committees preparing standards for consumer products or services; — regulators. This document is not applicable to bulk packaging, which is solely intended to protect products in bulk when being transported between manufacturers and retailers, and it is not intended for industrial packaging.

  • Guide
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This document specifies performance requirements and methods of test for non-reclosable packaging that have been designated child-resistant. This document is intended for type approval only (see 3.5) and is not intended for quality assurance purposes.

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  • Standard
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This document specifies performance requirements and methods of test for non-reclosable packaging that has been designated child-resistant and which is intended to contain non-pharmaceutical products. This document is intended for type approval only (see 2.5) and is not intended for quality assurance purposes. This document applies to non-reclosable packages of the single-use type consisting of one or more individual units. Non-reclosable packages for pharmaceutical products are excluded from the scope of this document. These are the subject of a separate standard, ISO 14375, Child-resistant non-reclosable packaging for pharmaceutical products — Requirements and testing.

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This part of IEC 60286 describes the common dimensions, tolerances and characteristics of
the tray. It includes only those dimensions that are essential for the handling of the trays for
the stated purpose and for placing or removing components from the trays.
Matrix trays are designed to facilitate the transport and handling of electronic components
during their testing, baking, transport/storage, and final mounting by automatic placement
equipment.
The generic rules for their design are given in this document. Newly developed trays that
follow these rules will not be listed individually. Only those trays that conform to the design
rules set forth herein are classified as "standard trays" and are thus preferred for use.
NOTE Matrix trays listed in Annex A that do not conform to the design rules set forth herein shall be considered
as "non-standard trays" and are not preferred for use.

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ISO 19809:2017 provides requirements and recommendations concerning accessible design of consumer packaging with regard to information and marking. This document specifies considerations and methods for designing and presenting information and marking to make consumer packages accessible to people with the widest range of capabilities by considering their sensory and cognitive abilities. This document applies to all types of information and marking presented on consumer packaging. Specifically excluded from this document are information and marking for medicinal products and medical devices including tamper verification. The design considerations and methods specified in this document are primarily intended for designers, developers and evaluators of packaging.

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ISO 15394:2017: - specifies the minimum requirements for the design of labels containing linear bar code and two-dimensional symbols on transport units to convey data between trading partners; - provides for traceability of transported units using a unique transport unit identifier (licence plate); - provides guidance on the formatting on the label of data presented in linear bar code, two-dimensional symbol or human-readable form; - provides specific recommendations regarding the choice of bar code symbologies, and specifies quality requirements; - provides recommendations as to label placement, size and the inclusion of free text and any appropriate graphics; - provides guidance on the selection of the label material. This document is not applicable to the direct printing on to kraft coloured corrugated surfaces. NOTE Guidance on the direct printing of bar code symbols on to kraft coloured corrugated surfaces are provided in references such as The Fibre Box Handbook[10].

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ISO 28219:2017 - defines minimum requirements for identifying items, - provides guidelines for item marking with machine-readable symbols, - covers both labels and direct marking of items, - includes testing procedures for label adhesive characteristics and mark durability, - provides guidance for the formatting on the label of data presented in linear bar code, two-dimensional symbol or human-readable form, - is intended for applications which include, but are not limited to, support of systems that automate the control of items during the processes of: - production, - inventory, - distribution, - field service, - point of sale, - point of care, - repair, and - is intended to include, but it is not limited to, multiple industries including: - automotive, - aerospace, - chemical, - consumer items, - electronics, - health care, - marine, - rail, - telecommunications. The location and application method of the marking are not defined (these will be reviewed and agreed upon by suppliers and manufacturers and their trading partners before implementing ISO 28219:2017). ISO 28219:2017 does not supersede or replace any applicable safety or regulatory marking or labelling requirements. ISO 28219:2017 is meant to satisfy the minimum item marking requirements of numerous applications and industry groups and as such its applicability is to a wide range of industries, each of which may have specific implementation guidelines for it. ISO 28219:2017 is to be applied in addition to any other mandated labelling direct-marking requirements. The labelling and direct marking requirement of ISO 28219:2017 and other standards can be combined into one label or marking area or appear as separate labels or marking areas. ISO 28219:2017 uses the terms "part marking" and "item marking" interchangeably. Unless otherwise stated, ISO 28219:2017 will use the term "item marking" to describe both the labelling and direct part marking (DPM) of an item, where DPM includes, but is not limited to, altering (e.g. dot peen, laser etch, chemical etch), as well as additive type processes (e.g. ink jet, vacuum deposition). The purpose of ISO 28219:2017 is to establish the machine-readable (linear, two-dimensional, and composite symbols) and human-readable content for direct marking and labelling of items, parts, and components. ISO 28219:2017 provides a means for items, parts and components to be marked, and read in either fixtured or hand-held scanning environments at any manufacturer's facility and then read by customers purchasing items for subsequent manufacturing operations or for final end use. Intended applications include, but are not limited to, supply chain applications, e.g. inventory, distribution, manufacturing, quality control, acquisition, transportation, supply, repair, and disposal. The figures are illustrative and not necessarily to scale or to the quality requirements specified in ISO 28219:2017.

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ISO/TS 17451-2:2017 specifies a common XML structure for the transmission of inventory information for shipments of household goods and personal effects between moving companies and their external partners. The Inventory XSD defined in Clause 5 specifies the XML structure to be used. Each XML document corresponds to one shipment carried by land, sea or air.

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ISO 19709-1:2016 specifies the essential characteristics and the common requirements and test methods for SLC systems used in the handling, transport and storage for the automotive industry. The application of such systems is described in Annex B. These containers are based on the modular area 600 mm × 400 mm, 550 mm × 366 mm and 600 mm × 500 mm and subdivisions according to ISO 3394 and ISO 3676. It is designed to be read in conjunction with the particular part which specifies the chosen system.

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ISO 21067-1:2016 specifies preferred terms and definitions related to packaging and materials handling, for use in international commerce, except for dangerous goods packaging where terms and definitions are given in the United Nations Recommendations on the Transport of Dangerous Goods [39]. ISO 21067-1:2016 is augmented by the following packaging-specific standards: - ISO 6590‑1; - ISO 6590‑2; - ISO 15867.

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ISO 17451-1:2016 relates to the moving of household goods and personal effects. It provides the codification of items and their condition, the transportation modes and associated data relating to a shipment. The relevant codes can be found in the related annexes and information regarding their use can be found in Clause 4. The objective of this document is to provide a common set of codes which allow movers of household goods and personal effects to exchange shipment-related information with each other and with external partners.

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ISO 780:2015 specifies a set of graphical symbols conventionally used for marking of distribution packages in their physical distribution chain to convey handling instructions. The graphical symbols should be used only when necessary.
ISO 780:2015 is applicable to packages containing any kind of goods, but does not include instructions specific to handling of dangerous goods.

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ISO 8317:2015 specifies performance requirements and test methods for reclosable packages designated as resistant to opening by children.
Acceptance criteria are given for the packages when tested by specified methods. These methods not only provide a measure of the effectiveness of the packaging in restricting access by children, but also cover the accessibility to the contents by adults.
ISO 8317:2015 is applicable to reclosable packages for any product intended to be exposed or removed from the packaging in normal use.
ISO 8317:2015 is intended for type approval only and is not intended for quality assurance purposes.

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ISO/TS 18614:2016 provides guidelines for users and suppliers providing the required information for requesting and specifying self-adhesive labels. It provides what to consider when defining and specifying label materials to be used for a given application. It will ensure that the relevant information is provided so that the right material for the intended application can be requested or recommended, as well as ensure that label parameters and characteristics are specified in a similar format to permit label materials to be requested, specified and compared in a consistent manner. It applies to labels with adhesive (also named as self-adhesive or pressure-sensitive). How to work and specify with other types of labels and marking are not addressed in ISO/TS 18614:2016, but may be the topic of subsequent documents. Also excluded is the information related to regulatory compliance.

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  • Technical specification
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ISO/TS 19709-3:2016 specifies the main characteristics and the testing of durable, reusable, parallelepipedic containers and their accessories which form a bond stackable system (BSS) designed to contain bulk or precisely located component loads up to maximum load of 20 kg used for automotive industry applications.

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ISO/TS 19709-2:2015 specifies the main characteristics and the testing of durable, reusable, parallelepipedic containers and their accessories which form a column stackable system (CSS) designed to contain bulk or precisely located component loads up to maximum load of 20 kg used for automotive industry applications.

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  • Technical specification
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This International Standard specifies a set of graphical symbols conventionally used for marking of
distribution packages in their physical distribution chain to convey handling instructions. The graphical
symbols should be used only when necessary.
This International Standard is applicable to packages containing any kind of goods, but does not include
instructions specific to handling of dangerous goods.

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This International Standard specifies performance requirements and test methods for reclosable
packages designated as resistant to opening by children.
Acceptance criteria are given for the packages when tested by specified methods. These methods not
only provide a measure of the effectiveness of the packaging in restricting access by children, but also
cover the accessibility to the contents by adults.
This International Standard is applicable to reclosable packages for any product intended to be exposed
or removed from the packaging in normal use.
This International Standard is intended for type approval only and is not intended for quality
assurance purposes.

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ISO 21067-2:2015 defines terms used in the field of packaging and the environment. It does not include terminology already covered by ISO 21067‑1 or other International Standards such as ISO 14050.

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ISO 780:2015 specifies a set of graphical symbols conventionally used for marking of distribution packages in their physical distribution chain to convey handling instructions. The graphical symbols should be used only when necessary. ISO 780:2015 is applicable to packages containing any kind of goods, but does not include instructions specific to handling of dangerous goods.

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ISO 8317:2015 specifies performance requirements and test methods for reclosable packages designated as resistant to opening by children. Acceptance criteria are given for the packages when tested by specified methods. These methods not only provide a measure of the effectiveness of the packaging in restricting access by children, but also cover the accessibility to the contents by adults. ISO 8317:2015 is applicable to reclosable packages for any product intended to be exposed or removed from the packaging in normal use. ISO 8317:2015 is intended for type approval only and is not intended for quality assurance purposes.

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This part of IEC 60286 applies to the tape packaging of components with two or more
unidirectional leads for use in electronic equipment. In general, the tape is applied to the
component leads.
It covers requirements for taping techniques used with equipment for automatic handling, preforming
of leads, insertion and other operations and includes only those dimensions which are
essential to the taping of components intended for the above-mentioned purposes.

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ISO 17480:2015 specifies requirements and recommendations for the accessible design for packaging with a focus on ease of opening. It applies to reclosable and non-reclosable consumer packaging without using any other mechanical means. This International Standard covers the design aspects addressing openability including opening location, opening methods, as well as evaluation techniques, both instrumented and user-based. This International Standard is primarily for designers, developers, and evaluators of packaging and will also be useful for other disciplines. For products regulated for safety or other reasons (e.g. toxic or dangerous goods and substances, medicinal products, and medical devices), those regulations take precedence.

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