HB 8413-2013
特殊过程确认的程序和要求
Procedure and requirements of special process validation
2013-04-25
T/NSSQ 049-2022
医疗器械清洁过程的开发、确认和常规控制的要求
2022-12-30
YY/T 1276-2016
医疗器械干热灭菌过程的开发、确认和常规控制要求
Requirements for the development,validation and routine control of dry heat sterilization process for medical devices
2016-03-23
BS ISO 16730-1-2015
Fire safety engineering. Procedures and requirements for verification and validation of calculation methods-General
消防安全工程 计算方法验证和确认的程序和要求
2015-08-31
T/CNS 9-2018
食品辐照-用电离辐射处理食品的辐照过程的开发、确认和常规控制要求
2018-03-15
IEC 62828-4-2020
Reference conditions and procedures for testing industrial and process measurement transmitters - Part 4: Specific procedures for level transmitters
工业和过程测量变送器试验的参考条件和程序.第4部分:液位变送器的特殊程序
2020-08-18
IEC 62828-2-2017
Reference conditions and procedures for testing industrial and process measurement transmitters - Part 2: Specific procedures for pressure transmitters
工业和过程测量变送器测试的参考条件和程序 - 第2部分:压力变送器的特殊程序
2017-11-07
GB/T 19633.2-2015
最终灭菌医疗器械包装 第2部分：成形、密封和装配过程的确认的要求
Packaging for terminally sterilized medical devices—Part 2: Validation requirements for forming, sealing and assembly processes
2015-12-10
YY/T 1464-2022
医疗保健产品灭菌 低温蒸汽甲醛 医疗器械灭菌过程的开发、确认和常规控制要求
Sterilization of health care products—Low temperature steam and formaldehyde—Requirements for development,validation and routine control of a sterilization process for medical devices
2022-10-17
GOST R 58633-2020
Системы и комплексы космические. Управление критичными и специальными процессами. Общие требования
空间综合体和系统 关键和特殊过程的控制 一般要求
GB/T 19974-2018
医疗保健产品灭菌 灭菌因子的特性及医疗器械灭菌过程的开发、确认和常规控制的通用要求
Sterilization of health care products—General requirement for characterization of a sterilization agent and the development,validation and routine control of a sterilization process for medical devices
2018-05-14
GB 18280.1-2015
医疗保健产品灭菌 辐射 第1部分:医疗器械灭菌过程的开发、确认和常规控制要求
Sterilization of health care products--Requirement for validation and routine control--Radiation sterilization
2015-12-31
GB 18278.1-2015
医疗保健产品灭菌 湿热 第1部分:医疗器械灭菌过程的开发、确认和常规控制要求
Sterilization of health care products--Requirements for validation and routine control--Industrial moist heat sterilization
2015-12-10
GB 18279.1-2015
医疗保健产品灭菌 环氧乙烷 第1部分:医疗器械灭菌过程的开发、确认和常规控制的要求
Medical devices--Validation and routine control of ethylene oxide sterilization
2015-12-10
T/CAQI 136-2020
产品质量鉴定程序规范电子和电气产品的特殊要求
DIN EN IEC 62828-3
Reference conditions and procedures for testing industrial and process measurement transmitters - Part 3: Specific procedures for temperature transmitters (IEC 62828-3:2018); German version EN IEC 62828-3:2018
工业和过程测量变送器的试验参考条件和程序.第3部分:温度变送器的特殊程序（IEC 62828-3-2018）；德国版本EN IEC 62828-3:2018
2019-02-01
DIN EN IEC 62828-2
Reference conditions and procedures for testing industrial and process measurement transmitters - Part 2: Specific procedures for pressure transmitters (IEC 62828-2:2017); German version EN IEC 62828-2:2018
工业和过程测量变送器试验的参考条件和程序.第2部分:压力变送器的特殊程序（IEC 62828-2-2017）；德国版本EN IEC 62828-2:2018
2018-11-01
DIN 25423-2
Sampling procedures for the monitoring of radioactivity in air - Part 2: Special requirements for sampling from air ducts and stacks
空气中放射性监测的取样程序第2部分:风管和烟囱取样的特殊要求
2000-08-01
GOST R 51385-1999
Элементы процедур передачи и форматы служебных пакетов (сообщений) в широкополосной цифровой сети интегрального обслуживания с быстрой коммутацией пакетов. Требования к процедурам и форматам
宽带综合业务数字网络中具有快速分组交换的业务分组（消息）的传输过程和格式的要素 对程序和格式的要求
AS/NZS ISO 16175.1-2021
Information and documentation - Processes and functional requirements for software for managing records, Part 1: Functional requirements and associated guidance for any applications that manage digital records
信息和文献.记录管理软件的过程和功能要求 第1部分:管理数字记录的任何应用程序的功能要求和相关指南
2021-03-19