55.020 - Packaging and distribution of goods in general
ICS 55.020 Details
Packaging and distribution of goods in general
Verpackung und Transport im allgemeinen
Emballage et distribution des marchandises en général
Pakiranje in distribucija blaga na splošno
General Information
Frequently Asked Questions
ICS 55.020 is a classification code in the International Classification for Standards (ICS) system. It covers "Packaging and distribution of goods in general". The ICS is a hierarchical classification system used to organize international, regional, and national standards, facilitating the search and identification of standards across different fields.
There are 416 standards classified under ICS 55.020 (Packaging and distribution of goods in general). These standards are published by international and regional standardization bodies including ISO, IEC, CEN, CENELEC, and ETSI.
The International Classification for Standards (ICS) is a hierarchical classification system maintained by ISO to organize standards and related documents. It uses a three-level structure with field (2 digits), group (3 digits), and sub-group (2 digits) codes. The ICS helps users find standards by subject area and enables statistical analysis of standards development activities.
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This document specifies the requirements and recommendations for establishing a traceability system for food in cold chain logistics, which enables integrated functions such as collecting traceability information, managing traceability information and implementing traceability. This document is applicable to the management processes by supporting food traceability whereas cold chain logistics service providers are needed, covering transportation, warehousing, loading and unloading and other related points in cold chain logistics links towards the end customers.
- Technical specification12 pagesEnglish languagesale 15% off
This document specifies test methods for the determination of the chemical compatibility of packaging/ IBC made from polyethylene (PE), fluorinated polyethylene and co-extruded plastics. It covers the determination of adequate plastics compatibility against the following processes of deterioration:
— softening due to absorption (swelling);
— stress cracking;
— combinations thereof.
This document is applicable to:
— drums and jerricans made from plastics;
— composite packaging (plastics) with inner receptacle made from plastics;
— rigid plastics IBCs (types 31H1 and 31H2);
— composite IBCs with rigid plastics inner receptacles (type 31HZ1);
used for the transport of liquid dangerous goods.
Proof of adequate plastics compatibility obtained using the test procedures specified in this document is only applicable to the above packaging and IBC types of the following materials and material specifications:
— packaging and IBCs made from PE;
— packaging and IBCs made from PE, whose internal surfaces are fluorinated; and
— packaging and IBCs which are coextrusion blow moulded and have walls with the following multilayer structure (from inside to outside):
— polyamide (PA), bonding agents, PE, or
— ethylene vinyl alcohol (EVOH), bonding agents, PE.
Note Packaging and IBCs made from PE and packaging and IBCs made from PE with fluorinated internal surfaces, deteriorate additionally due to molecular degradation reactions with the corresponding packaged substances. For this, the chemical compatibility can also be verified by the type tests described in ISO 13274:2013, Annex B, B.2.3, using the standard liquid nitric acid (55 %) or appropriate original packaged substances. Packaging made from Coex PE/PA and Coex PE/EVOH is not resistant to polar acid molecularly degrading substances such as nitric acid, with the result that a corresponding method is not considered for this process of deterioration in this document.
- Draft15 pagesEnglish languagee-Library read for1 day
This document specifies test methods for the determination of the chemical compatibility of packaging/ IBC made from polyethylene (PE), fluorinated polyethylene and co-extruded plastics. It covers the determination of adequate plastics compatibility against the following processes of deterioration: - softening due to absorption (swelling); - stress cracking; - combinations thereof. This document is applicable to: - drums and jerricans made from plastics; - composite packaging (plastics) with inner receptacle made from plastics; - rigid plastics IBCs (types 31H1 and 31H2); - composite IBCs with rigid plastics inner receptacles (type 31HZ1); used for the transport of liquid dangerous goods. Proof of adequate plastics compatibility obtained using the test procedures specified in this document is only applicable to the above packaging and IBC types of the following materials and material specifications: - packaging and IBCs made from PE; - packaging and IBCs made from PE, whose internal surfaces are fluorinated; and - packaging and IBCs which are coextrusion blow moulded and have walls with the following multilayer structure (from inside to outside): - polyamide (PA), bonding agents, PE, or - ethylene vinyl alcohol (EVOH), bonding agents, PE. Note Packaging and IBCs made from PE and packaging and IBCs made from PE with fluorinated internal surfaces, deteriorate additionally due to molecular degradation reactions with the corresponding packaged substances. For this, the chemical compatibility can also be verified by the type tests described in ISO 13274:2013, Annex B, B.2.3, using the standard liquid nitric acid (55 %) or appropriate original packaged substances. Packaging made from Coex PE/PA and Coex PE/EVOH is not resistant to polar acid molecularly degrading substances such as nitric acid, with the result that a corresponding method is not considered for this process of deterioration in this document.
- Standard10 pagesEnglish languagesale 15% off
- Standard11 pagesFrench languagesale 15% off
This document gives information on environmentally conscious packaging design based on the standards on packaging and the environment. It provides essential tips on how to improve packaging through reduction processes and includes practical examples to illustrate these points. This document is applicable to all suppliers responsible for placing packaging or packaged goods on the market.
- Technical report54 pagesEnglish languagesale 15% off
This document specifies the reference architecture for a hyperloop system. It specifies the functions of each (sub)system classifying them in different functional blocks, their different possible implementations, and highlights the interactions between them.
The interfaces of the transportation system based on interactions are listed, whether it be internal interfaces or exterior interfaces. The characterization considers the technical as well as operational features of the transport service.
- Standard17 pagesEnglish languagee-Library read for1 day
This document specifies requirements and guidelines for refrigerated storage services and refrigerated transport services for foods, in the business to business (B to B) logistics sector in order to ensure that cold chains are properly maintained. This document does not apply to logistics services for cosmetics, cigarettes, pharmaceutical and medical products, over-the-counter drugs and commercially available medicine. This document does not apply to customs operations. This document applies to environments where refrigeration must be created and maintained, and does not apply to environments needing to raise storage temperatures.
- Standard12 pagesEnglish languagesale 15% off
- Standard12 pagesFrench languagesale 15% off
- Standard12 pagesFrench languagesale 15% off
- Standard12 pagesFrench languagesale 15% off
This document specifies the reference architecture for a hyperloop system. It specifies the functions of each (sub)system classifying them in different functional blocks, their different possible implementations, and highlights the interactions between them.
The interfaces of the transportation system based on interactions are listed, whether it be internal interfaces or exterior interfaces. The characterization considers the technical as well as operational features of the transport service.
- Standard17 pagesEnglish languagee-Library read for1 day
This document specifies requirements for refrigerated delivery service providers to deliver goods directly from the last contactless refrigerated goods operation areas at distribution centres to recipients through contactless cold chain, depending on customers' needs. This document does not apply to the transfer of goods between distribution centres. This document includes requirements for: — refrigerated delivery service providers; — facilities and the equipment involved in contactless refrigerated delivery; — the operation process; — the handling of abnormal conditions. This standard is also applicable to scenarios that need contactless cold chain delivery under special circumstances, such as epidemics.
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- Standard12 pagesFrench languagesale 15% off
- Amendment7 pagesEnglish languagee-Library read for1 day
- Amendment7 pagesEnglish languagee-Library read for1 day
This document specifies the definitions, functional requirements and evaluation criteria of active packaging.
- Standard13 pagesEnglish languagesale 15% off
Hyperloop transport services are designed to support passenger transport and cargo transport. For each of the transport service user/customer requirements and expectations are different.
This document defines the hyperloop transport services supported by a hyperloop system and provides means for characterization and description of these services. The characterization considers the technical as well as operational / commercial features of each transport service.
- Standard33 pagesEnglish languagee-Library read for1 day
Hyperloop transport services are designed to support passenger transport and cargo transport. For each of the transport service user/customer requirements and expectations are different.
This document defines the hyperloop transport services supported by a hyperloop system and provides means for characterization and description of these services. The characterization considers the technical as well as operational / commercial features of each transport service.
- Standard33 pagesEnglish languagee-Library read for1 day
This document specifies a laboratory scale test method for determining the degree of disintegration of test items when exposed to well-managed home composting conditions by the weight evaluation method (WE method) using sieving and evaluation by weighing.
The test method is not applicable for the determination of the biodegradability of test items under home composting conditions. Additional testing is necessary for making claims concerning the suitability for home composting. This document is not appropriate for claims relating to the suitability for home composting.
This test method is carried out at laboratory scale under controlled conditions. Therefore, it does not reproduce any real home composting conditions, but it is devised to gain information on the potential of the test item to disintegrate sufficiently. A test item that passes this test is assumed to be capable of undergoing full disintegration in a 12 months home composting cycle carried out under well managed conditions. For features of well-managed home composting see EN 17427:2022, Annex E.
- Standard13 pagesEnglish languagee-Library read for1 day
SIGNIFICANCE AND USE
4.1 The purpose of this guide is to provide direction for uniform conditioning methodology when conducting special preparations of plastic packagings as prescribed for conducting United Nations (UN) drop test. This guide provides a uniform approach for conditioning of plastic packaging intended for liquid hazardous materials (dangerous goods).
4.2 The hazardous materials (dangerous goods) regulations certification process requires that plastic packagings undergo special preparations before performing the UN drop test. The regulations do not include uniform procedures for conducting special preparations. Non-uniform procedures allow for differences in methods between test facilities which may result in different test results.
4.3 49 CFR 178.603(c) state that special conditioning for drop testing is required for all plastic drums, plastic jerricans, plastic boxes (other than expanded polystyrene boxes), composite packagings (plastic material), and combination packagings with plastic inner packagings (other than plastic bags intended to contain solids or articles). It further states that drop testing shall be conducted when the temperature of the test sample (packagings and contents) has been reduced to –18 °C or lower. Test liquids shall be kept in the liquid state, if necessary, by the addition of antifreeze. Water/antifreeze solutions with a minimum 0.95 specific gravity for testing at –18 °C or lower are considered acceptable test liquids. These conditioning requirements also apply to IBCs and Large Packagings. Refer to 49 CFR §178.810(b)(4) and §178.965(c), respectively.
4.4 A 24-hour conditioning period may not be sufficient time for the packaging and contents to reach the required temperature.
4.5 This guide provides additional information not in the regulations that will facilitate consistent test sample conditioning among test facilities. The information and guidance provided here are intended to meet or exceed the minimum requirements of the regul...
SCOPE
1.1 This guide is intended to provide a standardized method and a set of basic instructions for special preparation conditioning of drop test samples being subjected to United Nations (UN) performance-oriented packaging certification as required by United States Department of Transportation Title 49 Code of Federal Regulations (49 CFR) and the United Nations Recommendations on the Transport of Dangerous Goods (UN).
1.2 This guide provides guidance on conditioning test samples for drop testing plastic Non-Bulk Packaging, Intermediate Bulk Container (IBC), and Large Packaging designs intended for liquid hazardous materials (dangerous goods) as required by 49 CFR §178.603(c)(1), §178.810(b)(4), and §178.965(c), respectively. This guide also provides the minimum information that should be documented when conducting special preparation conditioning.
1.3 The user of this guide shall be trained in accordance with 49 CFR §172.700 and other applicable hazardous materials regulations including: the International Civil Aviation Organization (ICAO) Technical Instructions for the Safe Transport of Dangerous Goods by Air, the International Maritime Dangerous Goods Code (IMDG Code), and carrier rules such as the International Air Transport Association (IATA) Dangerous Goods Regulations.
1.4 Units—The values stated in SI units are regarded as the standard. No other units of measurement are included in this standard.
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, G...
- Guide4 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
4.1 This design and evaluation guide describes multiple categories for evaluating flexible medical packages and packaging materials. These include safety, barrier, material and package performance attributes and characteristics, package integrity, visibility and appearance, processing, printed ink, distribution simulation, and conditioning.
4.2 The intent of this design and evaluation guide is to evaluate all cited categories and select those that are applicable. Once the product has been characterized and the sterilization methodology has been defined, there are numerous sets of requirements for any specific package. This design and evaluation guide provides an avenue for assessing these requirements and choosing test methods for both evaluating the package design and monitoring package compliance.
Note 1: Many of the standards included in this guide are consensus standards that are recognized by the United States Food and Drug Administration (FDA). Selection and use of a U.S. FDA recognized consensus standard is voluntary and the sole responsibility of the user in determining its applicability. For further information, consult the U.S. FDA Standards and Conformity Assessment Program at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatoryassistance/standards-and-conformity-assessment-program
4.3 Product characterization shall include mass or weight, geometry (length and width, height, and shape) and product composition.
4.4 All categories must be considered for applicability.
4.5 The Summary of Test Methods for Medical Packaging Design and Evaluation (Fig. 1) provides a compact graphical presentation of the test methods referenced in this guide.
SCOPE
1.1 This guide provides directions for the design and evaluation of primary flexible packages for medical products. The package materials must be selected appropriately for manufacturing process, end use, and the product being packaged.
1.2 This guide provides a compendium of test methods, practices, and procedures. Specific individual test methods must be selected based on the pertinent characteristics of the specific product to be packaged and the purpose for testing, research and development, or compliance. Not all test methods will be applicable.
1.3 This guide does not address acceptability criteria, which need to be determined jointly by the package producer and the medical products manufacturer.
1.4 This guide does not assess the product to be packaged or the sterilization method to be used.
1.5 The units cited in the referenced standard should be used.
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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- Guide27 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
4.1 This practice covers the requirements for the commercial preservation, packaging, packing (exterior container), unitization, and marking for supplies and equipment. It provides for multiple handling and shipment by any mode, and storage periods of a minimum of one year in enclosed facilities without degradation or damage to the product within the container. It also provides for package quantities suitable for redistribution without additional repackaging or marking. Planned storage that exceeds one year requires more than minimum requirements for physical and mechanical protection.
4.2 This practice is applicable to Department of Defense shipments for:
4.2.1 Items intended for immediate use;
4.2.2 Items for not-mission-capable supply;
4.2.3 Items intended for depot operational consumption;
4.2.4 Small parcel shipments (CONUS), not-for-stock; and
4.2.5 Direct vendor deliveries (CONUS ONLY).
4.3 All other Department of Defense shipments shall be in accordance with MIL-STD-2073–1.
SCOPE
1.1 This practice establishes minimum requirements for packaging of supplies and equipment, exclusive of ammunition, explosives, or hazardous materials, as covered in Title 49 of the Code of Federal Regulations.
1.2 The values stated in inch-pound units are to be regarded as standard. No other units of measurement are included in this standard.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
- Standard5 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
4.1 This practice provides:
4.1.1 A holistic approach to evaluate risks associated with an integrity breach in a SUS, considering its life cycle from development to disposal.
4.1.2 An overview of physical and microbial test methods that could be applicable to SUS testing, for qualification and validation purposes, as well as for routine testing.
4.1.3 Information on the main challenges faced when testing SUSs for integrity.
4.2 This practice can be used by SUS suppliers and SUS end users to define an integrity assurance strategy for SUSs, with the relevant tests when appropriate.
SCOPE
1.1 This practice uses quality risk management (QRM) and life-cycle approach to establish integrity assurance of single-use systems (SUSs), such as but not limited to bag assemblies and liquid transfer sets for processing, storage, and shipping of (bio)pharmaceutical products. It gives recommendations to identify failure modes and risks associated with such systems and their use-cases and how to identify the relevant leak(s) of concern. Integrity assurance in this context is limited to the barrier properties of the SUS, linked to microbial integrity and bioburden control (product quality) and liquid product loss (operator and environmental contamination). The required level of integrity assurance will depend on how critical the application is and can be interpreted in different ways. It can also vary between processes and applications used for different modalities (for example, advanced therapies). Other package barrier properties different from that, such as but not limited to gas barrier properties for gas headspace preservation, as well as porous barrier packages are not considered. Specific aspects how to address the contamination control strategy (CCS) for SUS are also described in chapters 8.131ff of the new Revision of Annex 1 (1),2 including chapter 8.137 regarding SUS integrity.
1.2 The test method overview provides descriptions that focus on the standard test setup and the identification of challenges in combination with SUSs. Details, including specific test setups, test parameter, and result interpretation, are not discussed. For more detailed information refer to Test Method E3251 for microbial test methods, and to Test Method E3336 for physical test methods.
1.3 This practice is not intended to apply to the use of single-use technology for primary containers, combination products (products composed of any combination of a drug, device, or biological product), or devices. Appropriate procedures related to these products are discussed in documents covering the integrity assurance for primary containers (2) or medical products (1, 3).
1.4 Techniques and procedures for complaint management and root cause analysis related to integrity failures are also not discussed.
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
- Standard13 pagesEnglish languagesale 15% off
- Standard13 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
4.1 Standards and practices for assuring safety, quality, and weight stabilization during key steps of the cannabis/hemp flowers sojourn are in order.
4.2 This guide is intended to assist in assuring safety, quality, and weight stabilization of cannabis/hemp flower during indoor packaging operations.
4.3 This guide is intended to assist in assuring that packaged cannabis/hemp flower has a water activity of 0.55 to 0.65 per Specification D8197.
4.4 This guide is intended to be used by purveyors who move the cured crop to consumer or non-consumer packaging used for distribution.
SCOPE
1.1 Specification D8450 specifies the environmental conditions, such as temperature, humidity, and lighting under which the cured, dry, cannabis/hemp flowers in fresh format intended for human use are to be packaged to assure the safety, quality, and weight stabilization of the packaged flower. This guide suggests means by which the packager of cannabis/hemp can meet Specification D8450.
1.1.1 This guide does not apply to frozen cannabis/hemp.
1.1.2 This guide does not apply to cannabis/hemp intended for extraction.
1.2 This guide applies only to controlling an indoor environment (heat, cooling, humidity control, lighting) surrounding packaging operations. Outdoor operations are outside the scope of this guide and are not addressed.
1.3 This guide can be used by licensed operators in the cannabis/hemp space who move the cured crop(s) into consumer or non-consumer packaging used for distribution.
1.4 Security of the cannabis/hemp flower during the packaging process is not within the scope of this guide.
1.5 This guide is intended to remain valid until the packaged cannabis/hemp flower is placed in storage or transit.
1.6 Authorities having jurisdiction may have additional or alternate requirements which shall take precedence or supersede this guide.
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
- Guide3 pagesEnglish languagesale 15% off
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.
- Standard22 pagesEnglish languagee-Library read for1 day
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.
- Standard21 pagesEnglish languagee-Library read for1 day
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.
- Standard22 pagesEnglish languagee-Library read for1 day
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.
- Standard21 pagesEnglish languagee-Library read for1 day
ABSTRACT
This guide identifies the key information required to ensure that selected packaging will pass the United Nations (UN) packaging certification at the level that is appropriate for its intended use. This guide covers test procedures for transportation of hazardous material packagings for net masses except those used for infectious substances, radioactive materials, cylinders, and other receptacles for gases and does not replace domestic or international requlatory requirements for hazardous material packagings. The UN performance tests are based on the degree of hazard posed by the proposed materials to be packaged which are also assigned to a specific packing group. Only packaging designs that meet the UN performance standards are to be marked with a UN mark. Tests include drop test, leakproofness test, stack test, vibration test, pressure differential test, hydrostatic pressure test, and cobb water absorption test.
SIGNIFICANCE AND USE
4.1 The UN performance tests are based on the degree of hazard presented by the proposed hazardous material(s) to be packaged.
4.2 Substances and articles which are hazardous are assigned to a specific packing group as defined in 3.8.1 and may be determined by referencing 49 CFR 172.101 hazardous materials table.
4.3 Only packaging designs that have been successfully tested to the UN performance standards as defined in 3.8.2 may have the UN specification mark applied to the outer packaging. Hazardous Materials may not be transported in a packaging that does not bear the appropriate UN specification markings unless otherwise authorized by the applicable competent authority.
4.4 Packages successfully tested to the UN performance standards may or may not withstand the North American distribution environment. To further evaluate the suitability of the package it is strongly recommended that additional tests as detailed in Practice D4169 or other carrier specified test requirements be conducted.
SCOPE
1.1 This guide identifies the key information required for United Nations (UN) packaging certification to ensure the selected packaging will be certified to the appropriate level for its intended use and provides guidance for locating relevant sections of the United States Department of Transportation Title 49 Code of Federal Regulations (CFR). Consult with a regulatory specialist whenever needed.
1.2 This guide provides assistance in determining the appropriate performance tests required to certify packaging designs to the United States Department of Transportation Title 49 Code of Federal Regulations performance oriented packaging standards based on the United Nations Recommendations on the Transport of Dangerous Goods..
1.3 This guide covers the testing for transportation of hazardous materials (dangerous goods) packagings for net masses not exceeding 400 kg (880 lb) or capacities not exceeding 450 L (119 gal), excepting packagings for infectious substances, radioactive materials, cylinders and other receptacles for gases.
1.4 This guide does not replace domestic or international regulatory requirements for hazardous materials packaging but is strongly recommended to be used in conjunction with those regulations.
1.5 The user of this guide must be trained in accordance with the United States Department of Transportation Title 49 Code of Federal Regulations (49 CFR) as required by 172.700 and should be familiar with other applicable hazardous materials regulations such as: International Civil Aviation Organization (ICAO) Technical Instructions for the Safe Transport of Dangerous Goods by Air, and the International Maritime Dangerous Goods Code (IMDG Code) and carrier rules such as International Air Transport Association (IATA) Dangerous Goods Regulations.
1.6 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not...
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- Guide10 pagesEnglish languagesale 15% off
SCOPE
1.1 This terminology is a compilation of definitions of technical terms used in the packaging and distribution environments. Terms that are generally understood or adequately found in other readily available sources are not included.
1.2 A definition is a single sentence with additional information included in discussions.
1.3 Definitions that are identical to those published by another standards organization or ASTM committee are identified with the name of the organization or ASTM committee.
1.4 The definitions in this terminology are grouped into related areas under principal concepts. The broad descriptor term for each group is followed in alphabetical order by narrower terms and related terms. Cross-references are included where the concept group is not obvious.
1.5 Terminology related to flexible barrier packaging is found in Terminology F17.
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
- Standard13 pagesEnglish languagesale 15% off
- Standard13 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
5.1 Regulations prescribing the test procedures for hazardous materials packaging allow for the substitution of non-hazardous fill materials for packaging performance tests with certain limitations prescribed and guidance offered (see 49 CFR 178.602(c)). This regulatory guidance has proven to be flexible enough, in common industry practice, to produce variations in the selection of fill materials for package performance tests sufficient to cause inconsistent and non-repeatable test results. This variation creates significant problems in product liability, packaging selection and regulatory enforcement in this highly regulated industry. Use of this guide should enhance uniformity in test procedures.
5.2 Consistent and repeatable test results coupled with clear test fill product descriptions will enhance transportation safety by simplifying packaging selection. This will also increase the general level of confidence that package testing, manufacture, and use are being guided by sound, generally accepted engineering principles. It also aids in clarifying expectations between the packaging industry and the regulatory authorities.
5.3 The guide will be used by packaging manufacturers and packaging test labs to create packaging test plans that meet customer needs and conform to the HMR. In addition, for the user of a packaging, certain information about the type and physical characteristics of the material used to test the packaging must be available in the test report and/or notification instruction to allow evaluation of whether a particular packaging was tested with a substitute material appropriate for the hazardous material to be shipped.
SCOPE
1.1 The purpose of this guide is to clarify the selection, use, and description criteria of non-hazardous particulate solid substitutes used to replace hazardous materials for the purpose of performance testing packagings. This includes identification of the physical parameters of substitute non-hazardous solid test fill materials that may affect packaging performance and test results and should be considered when selecting and describing a test fill material that conforms to the requirements of the Hazardous Materials Regulations (HMR). This guide is intended for use with package testing procedures for particulate solid materials that have flow characteristics. It is not intended for use with hazardous articles.
1.2 This guide provides information to assist packaging users, manufacturers, and performance testing service suppliers regarding the types of physical properties that should be considered when selecting substitute filling substances for the testing, certification and manufacture of packagings under the United Nations packaging protocols (UN Recommendations on the Transport of Dangerous Goods-Model Regulations) as adopted by US DOT in 49 CFR HMR.
1.3 This guide provides the suggested minimum information concerning the physical characteristics of the filling substances that should be documented in the certification test report and notification to users to allow for test repeatability and analysis, and to provide guidance to the user of a packaging of pertinent physical differences between potential hazardous lading and the filling substance with which the packaging was tested.
1.4 This guide does not purport to address regulatory requirements regarding the compatibility of filling substances with transport packagings. Compatibility requirements must be assessed separately, but it should be noted that under certain national and international dangerous goods regulations, the selection of the filling substances for package performance testing may be prescribed with respect to chemical compatibility requirements.
Note 1: Under the US HMR determination of packaging compatibility with a particular hazardous fill material is “the responsibility of the person offering the hazardous material for transportation” as prescribed in 49 CFR §...
- Guide6 pagesEnglish languagesale 15% off
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.
- Standard16 pagesEnglish languagesale 15% off
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.
- Technical report72 pagesEnglish languagee-Library read for1 day
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.
- Technical report72 pagesEnglish languagee-Library read for1 day
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.
- Standard37 pagesEnglish languagee-Library read for1 day
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.
- Standard53 pagesEnglish languagee-Library read for1 day
SIGNIFICANCE AND USE
5.1 This test method allows for the measurement of the torque retention properties of container/continuous thread closure systems of various designs, materials, and manufacture, and is suitable for package development and engineering evaluation.
5.2 Each test method can be used for the evaluation of non child resistant container/continuous thread closure systems under controlled conditions such as when the application torque is known and the applied downward force to the closure is zero or for Type I, style “A” push down and turn child resistant container/continuous thread closure systems under controlled conditions such as when the application torque and the applied downward force to the closure is known.
5.3 This test method measures torque retention properties of container/continuous thread closure systems with the use of an automated transducer based torque meter operating at a known rotational velocity (rpm) or known torque ramp.
5.4 This test method is intended for measurement of dry torque only.
SCOPE
1.1 These test methods evaluate the torque retention of continuous thread closures on containers with matching finishes, for predetermined environmental conditions over time. Methods are defined for both Type I, style “A” push down and turn Type II2 child resistant and non child resistant type closures.
1.2 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.
Note 1: The SI unit system is the recommended system.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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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.
- Standard53 pagesEnglish languagee-Library read for1 day
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.
- Standard24 pagesEnglish languagee-Library read for1 day
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.
- Standard44 pagesEnglish languagesale 15% off
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SCOPE
1.1 This standard specifies the environmental conditions, such as temperature, humidity, and lighting, under which cannabis/hemp flowers intended for human use are to be packaged to ensure the safety, quality, and weight stabilization of the packaged flower. This specification does not apply to frozen cannabis/hemp nor to cannabis/hemp intended for extraction.
1.2 This specification applies only to controlling an indoor environment (heat, cooling, humidity control) surrounding packaging operations. Outdoor operations are outside the scope of this specification and are not addressed.
1.3 This specification is to be followed by licensed operators in the cannabis/hemp space who move the cured crop(s) into consumer or non-consumer packaging used for distribution.
1.4 Security of the cannabis/hemp flower during the packaging process is not within the scope of this specification.
1.5 This specification is intended to remain valid until the packaged cannabis/hemp flower is placed in storage or transit.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
- Technical specification3 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
4.1 Shipping containers are exposed to complex dynamic stresses in the distribution environment. Approximating the actual damage, or lack of damage, experienced in real life may require subjecting the container and its contents to random vibration tests. In this way, many product and container resonances are simultaneously excited.
4.2 Resonance buildups during random vibration tests are less intense than during sinusoidal resonance dwell or sweep tests. Therefore, unrealistic fatigue damage due to resonance buildup is minimized.
4.3 Random vibration tests should be based on representative field data. When possible, confidence levels may be improved by comparing laboratory test results with actual field shipment effects. Refer to Practice D4169 for recommended random vibration tests. (See Appendix X1 and Appendix X2 for related information.)
4.4 There is no direct equivalence between random vibration tests and sinusoidal vibration tests. Equivalent tests between sine and random, in a general sense, are difficult to establish due to nonlinearities, damping and product response characteristics.
4.5 Vibration exposure affects the shipping container, its interior packing, means of closure, and contents. This test allows analysis of the interaction between these components. Design modification to one or all of these components may be used to achieve optimum performance in the shipping environment.
4.6 Random vibration tests may be simultaneously performed with transient or periodic data to simulate known stresses of this type, that is, rail joints, pot holes, etc.
4.7 Random vibration may be conducted in any axis (vertical or horizontal) or in any package orientation. However, different test levels may be utilized for each axis depending on the field environment that is to be simulated.
SCOPE
1.1 This test method covers the random vibration testing of filled shipping units. Such tests may be used to assess the performance of a container with its interior packing and means of closure in terms of its ruggedness and the protection that it provides the contents when subjected to random vibration inputs.
1.2 This test method provides guidance in the development and use of vibration data in the testing of shipping containers.
Note 1: Sources of supplementary information are listed in the Reference section (1-11).2
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific safety hazard statements are given in Section 6.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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SIGNIFICANCE AND USE
4.1 Many materials from which containers and packages are made, especially cellulosic materials, undergo changes in physical properties as the temperature and the relative humidity (RH) to which they are exposed are varied. Therefore, the package should be placed and kept in a specified atmosphere for a length of time such that subsequent measurements of physical properties will be meaningful and reproducible.
4.2 The conditions described in this practice are either historically accepted standard conditions or special laboratory conditions chosen to represent particular phases of the distribution environment. These special conditions do not necessarily duplicate actual field conditions, but tend to simulate them and have effects on packages and materials which may be related to their field performance.
SCOPE
1.1 This practice provides for standard and special conditioning and testing atmospheres that may be used to simulate particular field conditions that a container, package, or packaging component may encounter during its life or testing cycle.
1.2 This practice describes procedures for conditioning these containers, packages, or packaging components so that they approach or reach equilibrium with the atmosphere to which they may be exposed. This standard is commonly used for conditioning when conducting transit simulation tests.
1.3 Practice D685 should be used as the relevant conditioning standard when quantification of box compression strength at standard atmosphere conditions is required.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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- Standard3 pagesEnglish languagesale 15% off
This document provides guidelines for the cleaning and sanitation procedures for the sanitary operation of reusable transport packaging, which are used in the fields of handling, transport, storage and display of food and non-food products. It is applicable to all reusable transport items including reusable rigid plastic distribution boxes defined in ISO 18616-1.
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SIGNIFICANCE AND USE
4.1 Packages are often marked with handling instructions in the language of the country of origin. While this may safeguard the consignment to some extent, it is of little value for goods consigned to, or through, countries using different languages, and of no value at all if people unloading the packages are illiterate. Pictorial symbols offer the most likely means of conveying the consignor’s intention and their adoption will, therefore, undoubtedly reduce loss and damage through incorrect handling. The use of pictorial symbols does not provide any guarantee of satisfactory handling; proper protective packaging is therefore of primary importance.
SCOPE
1.1 This practice establishes a set of symbols to be used for marking of packages or containers to indicate special handling and storage requirements.
1.2 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units are provided for information only and are not considered standard.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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- Standard16 pagesEnglish languagesale 15% off
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.
- Technical specification36 pagesEnglish languagee-Library read for1 day
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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.
- Standard25 pagesEnglish languagee-Library read for1 day
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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SIGNIFICANCE AND USE
4.1 This practice is designed to determine the effects of different packaging materials whether of construction or systems (overpack, inert atmosphere, etc.), or both. Different packaging materials may require different packaging systems and thus detectable differences may not be experimentally separable from these influences. The practice then, is limited to those situations where comparative results are meaningful. This practice should be used where experimental materials or alternate storage conditions are evaluated against a known control, for example, a soft drink in cans with experimental liners versus known liners, or potato sticks in plastic bags versus coated paper bags. Accepted industry standard packages, such as glass bottles and metal cans may also be used as controls.
4.2 There are many ways in which a packaging material may influence a product during storage. First, the packaging material may contaminate the product with off-flavors/aromas by direct transfer of packaging component compounds to the product, commonly referred to as contribution or migration effect. Second, the packaging material may adsorb components from the product thus reducing flavor/aroma intensity of the product, commonly referred to as sorption or scalping effect. Third, external contaminants may permeate through the package and possibly be transferred into the product and/or compounds in the product may permeate out of the packaging, commonly referred to as permeation effect. (See Fig. 1.)
FIG. 1 Packing and Product Interactions Chart
SCOPE
1.1 This practice is designed to detect the changes in sensory attributes of foods and beverages stored in various packaging materials or systems, or both. It is not a practice intended to determine shelf-life.
1.2 This practice may be used for testing a wide variety of materials in association with many kinds of products. There are many ways in which a packaging material may influence a product during storage. First, the packaging material may contaminate the product with off-flavors by direct transfer of packaging component compounds to the product. Second, the packaging material may adsorb components from the product which may then be further transferred to the atmosphere, thus reducing aroma intensity in the product. Third, external contaminants may permeate the package and possibly be transferred to the product. In addition to flavor influences, packaging materials may allow color or textural changes, or both, and many other measurable sensory effects.
1.3 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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- Standard3 pagesEnglish languagesale 15% off
This document specifies requirements and provides guidance for the application, use and check of tamper verification features to the packaging of medicinal products.
- Standard25 pagesEnglish languagee-Library read for1 day
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].
- Standard67 pagesEnglish languagee-Library read for1 day
SIGNIFICANCE AND USE
5.1 There is no consistent method for the physical placement of an identifying label on equipment in the possession of an entity.
5.2 This practice is intended to expedite and improve the physical inventory and self-assessment processes and other occasions in which the instant identification of equipment is needed for purposes of control, management, or determining ownership, or a combination thereof.
5.3 The further intent of this practice is to reduce the administrative costs associated with activities requiring equipment identification, that is, physical inventory, self-assessments, and audits and to supplement Practice E2279, Practice E2452, and MIL STD 130.
SCOPE
1.1 This practice is for supplemental identification labels assigned by an entity and affixed to equipment to permit control.
1.2 Identifying labels include, but are not limited to, removable tags, bands, and plates.
1.3 This practice is not intended for material or manufacturer’s warranties.
1.4 This practice is not intended for markings of original equipment manufacturers (OEMs).
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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- Standard3 pagesEnglish languagesale 15% off
SIGNIFICANCE AND USE
5.1 Oxygen gas transmission rate is an important determinant of the protection afforded by barrier materials. It is not, however, the sole determinant, and additional tests, based on experience, must be used to correlate package performance with O2GTR. This test method is suitable as a referee method of testing, provided that the user and source have agreed on sampling procedures, standardization procedures, test conditions, and acceptance criteria.
SCOPE
1.1 This test method covers a procedure for the determination of the steady-state rate of transmission of oxygen gas into packages. More specifically, the method is applicable to packages that in normal use will enclose a dry environment.
1.2 The values stated in SI units are to be regarded as the standard.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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- Standard7 pagesEnglish languagesale 15% off
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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