C04 基础标准与通用方法 标准查询与下载

DB4403/T 33-2019 轮椅车位支撑装置适配技术规范

本标准适用于深圳市提供轮椅支撑装置适配的技术。

Wheelchair parking space support device adaptation technical specification

DB45/T 1974-2019 瑶医风敌症诊疗技术规范

Diagnosis and treatment technical specifications for wind enemy disease in Yao medicine

DB33/T 2194-2019 体质测定与健身指导技术规范

Physical fitness determination and fitness guidance technical specifications

DB33/T 2239-2020 经颅磁刺激戒毒康复应用管理规范

Application management specification of transcranial magnetic stimulation for detoxification and rehabilitation

DB5101/T 34-2018 老年护理常见风险防控指南

本标准规定了老年护理常见风险要求的术语和定义、常见风险、基本要求、防控指南。 本标准适用于成都市行政区域内养老服务组织、提供医养结合服务的医疗机构中的老年护理常见风 险的防控指南。

Guidelines for the Prevention and Control of Common Risks in Elderly Care

DB5101/T 35-2018 成都市养老机构医养结合建设规范

本标准规定了成都市养老机构医养结合建设的术语与定义、医养结合功能基本配置、基本要求、养老机构医务室基本标准、养老机构护理站基本标准、养老机构康复室基本标准、养老机构增设护理院或护理中心、养老机构增设康复机构、养老机构与医疗机构合作、管理要求、评估评价。 本标准适用于成都市行政区域内，经政府有关部门依法登记、提供医养结合服务的养老机构。

Regulations on the Construction of Combination of Medical and Elderly Care in Chengdu Elderly Care Institutions

DIN EN ISO 11137-3:2017 保健产品的灭菌.辐射.第3部分:发展、验证和常规控制剂量方面的指导(ISO 11137-3-2017);德文版本EN ISO 11137-3-2017

ISO 11137-3 gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a radiation sterilization process.

Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017); German version EN ISO 11137-3:2017

DB44/T 2016-2017 水中6种环境雌激素类化合物的测定固相萃取-高效液相色谱-串联质谱法

本标准规定了测定水中6种环境雌激素类化合物的固相萃取-高效液相色谱-串联质谱法。 本标准适用于地表水、地下水和污水中炔雌醇、雌酮、17β-雌二醇、雌三醇、4-n-辛基酚和4-n-壬基酚6种环境雌激素类化合物的测定。 当富集样品体积为1000 mL，浓缩后定容体积为1.0 mL，进样体积为10 μL时，本方法的检出限为0.6~0. 9 ng/L，测定下限为2.4~3.6 ng/L，应按附录A执行。

Determination of six environmental estrogenic compounds in water by solid-phase extraction-high performance liquid chromatography-tandem mass spectrometry

ISO 11137-3:2017 保健产品的灭菌.辐射.第3部分:发展、验证和常规控制剂量方面的指导

This document gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in radiation sterilization process.

Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control

DB33/T 2030-2017 人间充质干细胞库建设与管理规范

Standards for construction and management of human mesenchymal stem cell bank

DIN 12980:2017 实验室装置. 细胞毒性物质和其他CMR药物的安全柜和手套箱

Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs

BS ISO 18562-1:2017 医疗保健应用中呼吸气体通道的生物相容性评估 风险管理过程中的评估和测试

Biocompatibility evaluation of breathing gas pathways in healthcare applications. Evaluation and testing within a risk management process

BS ISO 18562-4:2017 医疗保健应用中呼吸气体通道的生物相容性评估. 冷凝物中析出物试验

Biocompatibility evaluation of breathing gas pathways in healthcare applications. Tests for leachables in condensate

BS ISO 18562-3:2017 医疗保健应用中呼吸气体通道的生物相容性评估. 挥发性有机化合物(VOC)排放试验

Biocompatibility evaluation of breathing gas pathways in healthcare applications. Tests for emissions of volatile organic compounds (VOCs)

BS ISO 18562-2:2017 医疗保健应用中呼吸气体通道的生物相容性评估. 颗粒物排放试验

Biocompatibility evaluation of breathing gas pathways in healthcare applications. Tests for emissions of particulate matter

DB33/T 2028-2017 海域基准价核定规程

Regulations for the verification of benchmark prices in sea areas

ASTM D7372-17 熟练试验程序结果的分析和说明用标准指南

5.1 This guide can be used to evaluate the performance of a laboratory or group of laboratories participating in a proficiency test (PT) program involving petroleum and petroleum products. 5.2 Data accrued, using the techniques included in this guide, provide the ability to monitor analytical measurement system precision and bias. These data are useful for updating standard test methods, as well as for indicating areas of potential measurement system improvement for action by the laboratory. This guide serves both the individual participating laboratory and the responsible standards development group as follows: 5.2.1 Tools and Approaches for Participating Laboratories. Administrative Reviews Flagged Data and Investigations Data Normality Checks QQ Plots Histograms Bias (Deviation from Mean) Z-Scores, Z′-Scores Trends Precision Performance—TPIIND, F-test Comparison of PTP and Individual Laboratory Site Precision 5.2.2 Tools and Approaches for Responsible Standards Development Groups. TPI and precision trends Bias and precision comparisons via box & whisker plots Normality evaluations Relative standard deviations Uncontrolled variables 5.3 Reference is made in this guide to the ASTM International Proficiency Test Program on Petroleum Products, Liquid Fuels, and Lubricants, version PTP 2.0 implemented in 2016–2017. Program reports containing similarly displayed results and statistical treatments may be available in other PT programs. Appendix X2 summarizes the statistical tools referenced in this guide and Appendix X3 is a collection of examples covering many of the approaches described in this guide. 1.1 This guide covers the evaluation and interpretation of proficiency test program (PTP) results. For proficiency test program participants, this guide describes procedures for assessing participants’ results relative to the collective PT program results and potentially improving the laboratory’s testing performance based on the assessment of findings and insights. For the committees responsible for the test methods included in PT programs, this guide describes procedures for assessing industry’s ability to perform test methods and for potentially identifying opportunities for improvements. 1.2 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. 1.3 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Prin......

Standard Guide for Analysis and Interpretation of Proficiency Test Program Results

ASTM E1588-17 采用扫描电子显微术/能量散射X射线光谱法进行射击残留物分析的标准实施规程

5.1 This document will be of use to forensic laboratory personnel who are involved in the analysis of GSR samples by SEM/EDS (5). 5.2 SEM/EDS analysis of GSR is a non-destructive method that provides (6, 7) both morphological information and the elemental profiles of individual particles. 5.3 Particle analysis contrasts with bulk sample methods, such as atomic absorption spectrophotometry (AAS) (8), neutron activation analysis (NAA) (9), inductively coupled plasma atomic emission spectrometry (ICP-AES), and inductively coupled plasma mass spectrometry (ICP-MS), where the sampled material is dissolved or extracted prior to the determination of total element concentrations, thereby sacrificing size, shape, and individual particle identification. 1.1 This practice covers the analysis of gunshot residue (GSR) by scanning electron microscopy/energy-dispersive X-ray spectrometry (SEM/EDS) using manual and automated methods. The analysis may be performed manually, with the operator manipulating the microscope controls and the EDS system software, or in an automated fashion, where some amount of the analysis is controlled by pre-set software functions. This practice refers to the analysis of electron microscopy stubs and does not address sample collection (1).2 1.2 Since software and hardware formats vary among commercial systems, guidelines will be offered in the most general terms possible. For proper terminology and operation, consult the SEM/EDS system manuals for each instrument. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.4 This practice offers a set of instructions for performing one or more specific operations. This practice cannot replace knowledge, skill, or ability acquired through appropriate education, training, and experience and should be used in conjunction with sound professional judgment. 1.5 This practice does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user when applying this practice to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Standard Practice for Gunshot Residue Analysis by Scanning Electron Microscopy/Energy Dispersive X-Ray Spectrometry

DB45/T 1411-2016 瑶医疾病四态分型规范

Yao medical disease four-state classification standard

JIS T 0801:2016 卫生保健品灭菌.环氧乙烷.医疗设备消毒过程的制定、确认和常规控制的要求

Sterilization of health care products -- Ethylene oxide -- Requirements for the development, validation and routine control of a sterilization process for medical devices