01.040.11 医药卫生技术(词汇) 标准查询与下载

DB45/T 2631-2023 肌筋膜触发点治疗技术规范

Myofascial trigger point therapy technical specification

ASTM D8270-23 与大麻有关的标准术语

1.1 This terminology is a compilation of definitions of technical terms used in the cannabis industry. Terms that are generally understood or adequately defined in other readily available sources are not included. 1.2 When a term is used in an ASTM document for which Committee D37 is responsible it is included only when judged, after review by Subcommittee D37.91, to be a generally usable term. 1.3 Definitions that are identical to those published by other ASTM committees or other standards organizations are identified with the committee number (for example, D20) or with the abbreviation of the name of the organization (for example, IUPAC, International Union of Pure and Applied Chemistry). 1.4 A definition is a single sentence with additional information included in discussions. 1.5 Definitions are followed by the committee responsible for the standard(s) (for example, [D37.01]) and standard designation(s) in which they are used (for example, D8219). 1.6 Abbreviated Terminology: 1.6.1 Abbreviated terminology is intended to provide uniform contractions of terms relating to cannabis that have evolved through widespread common usage. The compilation in this standard has been prepared to avoid the occurrence of more than one abbreviated term for a given cannabis term and to avoid multiple meanings for abbreviated terms. 1.6.2 The abbreviated terminology and descriptions in this standard are intended to be consistent with usage in the cannabis industry and the standards under D37 jurisdiction. Other ASTM committees may assign a different word-phrase description to the same abbreviated terminology. In such cases, the abbreviated terms in this standard shall apply to usage in D37 standards, or if widespread misunderstanding could result from conflicting abbreviated terminology descriptions, the abbreviated terminology for the word-phrase shall not be used in D37 standards. 1.6.3 Acronyms and Initialisms—A word formed from the letters or parts of words of a longer word-phrase, usually from the initial letters or parts of the words. An acronym is pronounced as a word (for example, radar for radio detection and ranging). An initialism is pronounced as a series of letters (for example, DOT for Department of Transportation). 1.6.4 The acronym or initialism description is the origin word-phrase for the acronym or initialism, not a definition. 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.

Standard Terminology Relating to Cannabis

ASTM F1638-95(2023) 外科组织/敷料/拾取钳（拇指型）的标准术语

1.1 This terminology defines basic terms and considerations for components of thumb-type surgical forceps. Instruments with this terminology are limited to those fabricated from stainless steel and used for surgical procedures. 1.2 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 Terminology for Surgical Tissue/Dressing/Pick-Up Forceps (Thumb-Type)

ASTM F1840-10(2023) 外科缝合针的标准术语

1.1 This terminology covers general definitions for surgical needles. 1.2 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 Terminology for Surgical Suture Needles

ASTM E2363-23 制药和生物制药工业中制药和生物制品制造相关的标准术语

1.1 This standard covers terminology used by the E55 Committee relating to pharmaceutical and biopharmaceutical industry for manufacture of pharmaceutical and biopharmaceutical products. Terms that are generally understood and in common usage or adequately defined in other readily available references are not included except where particular delineation to pharmaceutical and biopharmaceutical manufacturing may be more clearly stated. 1.2 This terminology is, therefore, intended to be selective of terms used generally in the manufacture of pharmaceutical and biopharmaceutical products and published in a number of documents such as those listed in the succeeding section. The listing is also intended to define terms that appear prominently within other related ASTM International standards and do not appear elsewhere. 1.3 The definitions are substantially identical to those published by regulatory agencies such as the U.S. Food and Drug Administration, European Medicines Agency, Pharmaceutical and Medical Devices Agency (Japan), other and national competent authorities (human) as well as other authoritative bodies, such as ICH, ISO, and national standards organizations. 1.4 This terminology supplements current documents on terminology that concentrate on the manufacture of pharmaceutical and biopharmaceutical products. 1.5 An increasing number of product designations and designations for chemical, physical, mechanical, analytical, and statistical tests and standards are coming into common usage in the literature, regulatory environment, and commerce associated with the manufacture of pharmaceutical and biopharmaceutical products. 1.6 Units—The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard. 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.

Standard Terminology Relating to Manufacturing of Pharmaceutical and Biopharmaceutical Products in the Pharmaceutical and Biopharmaceutical Industry

T/GDPMAA 0009-2022 人类疾病模型技术体系

本标准提出了关于人类疾病模型精准应用的术语和定义、体系框架、核心技术及应用、技术路径和伦理考虑。

The Technology System of Human Diseases Model

T/AHPCA 042-2022 垫类保健用品

本标准规定了垫类保健用品技术规范，主要包括术语和定义、结构组成、指标要求、试验方法、特别说明、标志、标签、包装、运输及贮存等内容。 本标准适宜于直接或者间接作用于人体皮肤表面，不以预防和治疗疾病为目的，具有日常保健功能的垫类保健用品。

Pad health care products

DB41/T 2318-2022 药品批发企业现代物流基本要求

本文件规定了药品批发企业现代物流的组织机构与人员、场所设置、设施与设备、校准与验证、信息管理系统和质量管理体系要求。 本文件适用于药品批发企业(以下简称“企业”) 现代物流的开办与管理。

Basic Requirements for Modern Logistics of Pharmaceutical Wholesale Enterprises

T/HBJY 004-2022 中医药非遗外用衍生品通用技术规范

本文件规定了中医药非遗外用衍生品的术语和定义、要求、试验方法、检验规则、评估备案、标志、标签和说明书、包装、运输和贮存、保质期。

General Technical Specifications for External Use Derivatives of Intangible Cultural Heritage of Traditional Chinese Medicine

T/ZGKSL 001-2022 人体皮肤衰老评价标准

本标准规定了：皮肤衰老的术语、定义、临床表现、严重度分级；皮肤无创性测量技术评价皮肤衰老图像、二维、三维影像和生理学等参数指标；皮肤衰老相关的组织学、基因和蛋白质等评价技术和参数。

Evaluation criteria for human skin aging

T/JPMA 016-2022 致病性弧菌和类志贺邻单胞菌的检测 多重PCR-毛细管电泳法

本文件规定了一种可同时检测霍乱弧菌（Vibrio cholerae）、副溶血性弧菌（Vibrio parahaemolyticus）、河弧菌（Vibrio fluvialis）、拟态弧菌（Vibrio mimicus）、创伤弧菌（Vibrio vulnificus）和类志贺邻单胞菌（Plesiomonas shigelloides）的多重PCR-毛细管电泳法。 本文件适用于粪便标本、水产品、环境水体中霍乱弧菌、副溶血性弧菌、河弧菌、拟态弧菌、创伤弧菌和类志贺邻单胞菌的快速定性检测。

Detection of pathogenic Vibrio and Plesiomonas shigelloides Multiplex PCR-capillary electrophoresis

DB13/T 5602-2022 医学影像学大数据智能应用技术指南

Technical guide for intelligent application of big data in medical imaging

DB32/T 4271-2022 医疗器械洁净室（区）检验规范

本文件规定了医疗器械洁净室（区）检验人员的要求及准备工作、技术要求及检验方法。 本文件适用于医疗器械洁净室（区）空气洁净度的检验。

Medical device clean room (area) inspection specification

T/HARACM 0006-2022 膏剂类健康用品生产技术规范

1  范围　 2  规范性引用文件　 3  术语和定义　 4  技术要求　 5  试验方法　 6  检验规则　 7  使用方法　 8  健康功能　 9  注意事项　 10  规格　 11  评审认证　 12  标签 包装 运输 储存和保质期　

Technical Code for production of paste health products

T/HARACM 0005-2022 粉剂类健康用品生产技术规范

1  范围　 2  规范性引用文件　 3  术语和定义　 4  技术要求　 5  试验方法　 6  检验规则　 7  使用方法　 8  健康功能　 9  注意事项　 10  规格　 11  评审认证　 12  标签 包装 运输 储存和保质期　

Technical Code for production of powder health products

T/HARACM 0002-2022 贴敷类健康用品生产技术规范

1  范围　 2  规范性引用文件　 3  术语和定义　 4  技术要求　 5  试验方法　 6  检验规则　 7  使用方法　 8  健康功能　 9  注意事项　 10  规格　 11  评审认证　 12  标签 包装 运输 储存和保质期　

Technical Code for the production of sticking and applying health products

T/HARACM 0001-2022 健康用品生产技术规范

1  范围　 2  规范性引用文件　 3  术语和定义　 4  技术要求　 5  试验方法　 6  检验规则　 7  使用方法　 8  健康功能　 9  注意事项　 10  规格　 11  评审认证　 12  标签 包装 运输 储存和保质期　

Technical Code for production of health products

ISO/TS 6304:2022 中医-疾病的分类结构

Traditional Chinese medicine — Categorial structure for disorders

T/CPAPE 01-2022 采用吹灌封（BFS）技术生产无菌产品 通用技术要求

本文件依据《药品生产质量管理规范》（2010年修订）中附录一无菌药品中第17条和第18条的要求，并参考了“美国注射剂协会（PDA)第77号技术报告《运用吹灌封技术制造无菌药品》、国际吹灌封操作者协会《利用吹灌封技术进行无菌药品和输液产品生产的考虑点》2012版以及“USP 43/44 第1116章节中关于先进无菌技术”“无菌生产工艺环境的洁净级别”的内容。

The Manufacture of Sterile Products Using Blow-Fill-Seal Technology

T/CACM 1388-2022 湿证评估操作规程

前言 ………………………………………………………………………………………………………… Ⅰ 引言 ………………………………………………………………………………………………………… Ⅱ 1 范围 ……………………………………………………………………………………………………… 1  2 规范性引用文件 ………………………………………………………………………………………… 1  3 术语和定义 ……………………………………………………………………………………………… 1 4 湿证的评估流程及评估方法 …………………………………………………………………………… 4  4.1 评估工具 …………………………………………………………………………………………… 4  4.2 操作流程 …………………………………………………………………………………………… 4  4.3 评估方法 …………………………………………………………………………………………… 5  附录 Ａ （规范性） 中医湿证评估量表 …………………………………………………………………… 6  附录Ｂ（规范性） 中医湿证评估量表维度划分 ………………………………………………………… 8  参考文献 …………………………………………………………………………………………………… 10

Operating procedure for dampness syndrome evaluation