55.020 货物的包装和调运综合 标准查询与下载

DB3205/T 1102-2023 绿色快递服务中心等级评定规范

Green Express Service Center Grade Rating Standards

DB3401/T 305-2023 药品多仓一体化管理规范

Pharmaceutical multi-warehouse integrated management specifications

KS T 6012-2023 聚对苯二甲酸乙二醇酯饮料瓶制造质量试验方法

Manufacturing quality test methods for polyethylene terephthalate beverage bottles

ASTM D7790-19(2023) 联合国（UN）跌落试验用含液体塑料包装的制备标准指南

Standard Guide for Preparation of Plastic Packagings Containing Liquids for United Nations (UN) Drop Testing

T/CPF 0075-2023 汽车成套零部件出口包装通用技术要求

本文件规定了汽车成套零部件出口包装的基本原则与要求、包装设计要求、包装选用规则、包装编号规则、包装尺寸系列、包装强度要求以及零部件分类及包装防护要求。

General technical requirements for export packaging of automotive knocked down parts

ASTM D3951-18(2023) 商业包装标准实施规程

Standard Practice for Commercial Packaging

ISO/CD 4924:2023 邮寄和递送包装的生态设计原则、要求和指南

Eco-design principle, requirement and guideline for posting and delivery packaging

T/QGCML 1383-2023 环保型温变标签

本文件规定了环保型温变标签的术语定义、技术要求、试验方法、检验规则、标志、包装、运输及贮存。 本文件适用于环保型温变标签的生产和验收。

Environmentally friendly temperature change label

ISO/DIS 31512:2023 企业对企业 (B to B) 领域的冷链物流服务 – 存储和运输的要求和指南

Cold chain logistics services in Business to Business (B to B) sector – Requirements and guidelines for storage and transport

ASTM E3244-23 一次性系统完整性保证和测试的标准实践

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.

Standard Practice for Integrity Assurance and Testing of Single-Use Systems

KS T 5055-2023 包装.完整的、装满的运输包装.包裹递送用包装产品的试验方法

Packaging — Complete, filled transport packages — Test methods for packaged product for parcel delivery

T/HBCC 011-2023 河北净菜配送规范

本文件规定了“河北净菜”配送基本要求、设施设备、配送流程、配送作业要求、服务和管理质量要求。适用于“河北净菜”的配送。

Hebei Clean Vegetable Distribution Specifications

T/CASME 492-2023 产品包装设计通用技术要求

本文件规定了产品包装设计的术语和定义、基本要求、设计原则、设计因素、确定设计方案、材料选择、尺寸和结构、法规要求和可持续性要求技术内容。

General technical requirements for product packaging design

T/ZSHG 016-2023 气雾剂抗冲击试验测试方法

4　测试方法 4.1　仪器设备 4.1.1 抗冲击测试仪，如图1  抗冲击测试仪示意图所示：1-1底座500mm，1-2高度2000mm，1-3跌落冲击板; 4.1.2 压力表：量程 0~1.6 MPa，精度不低于1.6级，带专用接头； 4.1.3 高速摄像仪； 4.1.4 恒温水浴：控温精度±1℃； 4.1.5 卷尺：精度±1mm； 4.2　试样的准备 4.2.1 气雾剂试样（下称试样）所采用的容器、阀门应经检验合格，符合GB 13042  包装容器 铁质气雾罐及GB/T 17447 气雾阀要求。 4.2.2 试样的容器、阀门结合密封后，其封口直径、深度应检查合格。 4.2.3 试样经50℃肥皂水浸泡，3min之内目测无气泡产生，其内压应低于容器和阀门允许的使用压力，肥皂水的制作方法按4.5.1的要求进行；相关项目按GB/T 14449  气雾剂产品测试方法执行； 4.2.4 试样内容物、抛射剂、净质量、充填率按实际产品及测试方案要求。 4.2.5 批量抽取试样可按GB/T 2828执行或按试样不小于6罐。 4.3　测试步骤 4.3.1 取6罐试样，记录产品抗冲击试验前的内压（MPa）、罐身高度（mm）、材质参数等资料。 4.3.2 将试样置于恒温水浴（25℃）不小于30min，测试须在样品恒温后3min内完成。 4.3.3 戴厚皮手套，取出试样。除试样标明不允许摇动罐体外，摇动试样6次。 4.3.4 抗冲击测试仪高度调节固定在垂直距离(2000±2)mm处。 4.3.5 自由跌落角度固定在45°范围内。 4.3.6 试样垂直放置抗冲击试验仪平台上平稳，启动开关，试样垂直跌落，准确跌落到跌落冲击板设定位置，跌落冲击板与水平成一定角度。 4.3.7 通过高速摄像仪拍摄图像，确认气雾罐与垂直跌落冲击钢板情况，避免其他原因导致冲击角度不良而影响试验结果。 4.3.8 测试6个试样，试样测试的结果合格率即为该产品的抗冲击性能(评判标准按4.5要求)。 4.4　注意事项 4.4.1 测试区域符合GB50016-2014 规定，应无明火，并配置灭火器材。 4.4.2 测试应在无风、地面平整区域进行。 4.4.3 抗冲击试验时无关人员禁止进入测试区域。 4.4.4 测试人员须作适当安全防护，防止因爆罐造成伤害。 4.4.5 若气雾剂产品发生爆罐或泄漏，应适时清理仪器设备上残留物。 4.5　结果判定 4.5.1 安全测试：将肥皂放置于称量纸上，用剪刀轻轻地刮肥皂，让肥皂沫落在称量纸上，接着将称量纸上的肥皂沫倒入杯子中，往杯子中倒入清水，肥皂沫与水按重量比为1:10，用玻璃棒搅拌杯子中的溶液，使肥皂沫完全溶解制成肥皂水，用刷子刷在罐子试样全身，没有泡泡吹起来为合格。 4.5.2 性能测试：预先将恒温水浴调至（50±1）℃，将摇匀后并脱去防护盖的试样，浸泡于恒温水浴中，5min内每罐试样冒出气泡不应该超过5个，5min后没有气泡冒出为合格。

Test method for aerosol impact resistance test

ISO/CD 31511:2023 冷链物流无接触配送服务要求

Requirements for contactless delivery services in cold chain logistics

ISO/CD TR 22251-1:2023 可回收运输物品上使用 RFID 的应用指南 第 1 部分：金属可回收运输物品

Application Guideline for use of RFID on Returnable Transport Items — Part 1: For metal returnable transport items

BS EN ISO 28862:2023 包装 儿童安全包装 非药品不可重新封闭包装的要求和测试程序

1   Scope 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.

Packaging. Child-resistant packaging. Requirements and testing procedures for non-reclosable packages for non-pharmaceutical products

BS EN ISO 14375:2023 用于药品的儿童安全且不可重新封闭的包装 要求和测试

Child-resistant non-reclosable packaging for pharmaceutical products. Requirements and testing

T/CIET 074-2023 绿色包装评价通则

本文件规定了绿色包装评价要求、评价方法、评价报告内容和格式。 本文件适用于绿色包装的评价。

General Rules for Green Packaging Evaluation

ISO/CD 31512 to B部门的冷链物流服务 低温仓储服务和低温运输服务要求

Cold chain logistics services in B to B sector — Requirements for low temperature storage services and low temperature transport services