DIN 58341-DRAFT
Draft Document - Requirements for the validation of cleaning and disinfection processes
文件草案-清洁和消毒过程验证要求
2019-09-01
AAMI ST98-2022
Cleaning validation of health care products - Requirements for development and validation of a cleaning process for medical devices
保健产品的清洁验证.医疗器械清洁工艺的开发和验证要求
2022-08-22
GB/T 43731-2024
生物样本库中生物样本处理方法的确认和验证通用要求
General requirements for the validation and verification of processing methods for biological material in biobanks
2024-03-15
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
BS ISO 21899-2020
Biotechnology. Biobanking. General requirements for the validation and verification of processing methods for biological material in biobanks
生物技术 生物银行 生物库中生物材料加工方法验证和验证的一般要求
2020-06-25
KS J ISO 21899
생명공학기술 — 생물자원은행 운영 — 생물자원은행에서의 생물자원 처리 방법에 대한 유효화 및 검증에 대한 일반 요구사항
生物技术.生物库.生物库中生物材料加工方法验证和验证的一般要求
2023-04-18
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
ISO 21899-2020
Biotechnology — Biobanking — General requirements for the validation and verification of processing methods for biological material in biobanks
生物技术.生物银行.生物银行中生物材料加工方法的验证和验证的一般要求
2020-06-15
BS PD ISO/TS 21387-2020
Sterilization of medical devices. Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release
医疗器械的消毒 使用参数释放的环氧乙烷灭菌过程的验证和常规处理要求指南
2020-09-16
ISO/TS 21387-2020
Sterilization of medical devices — Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release
医疗器械的灭菌 - 使用参数释放对环氧乙烷灭菌过程的验证和常规加工要求的指导
2020-09-15
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
ISO 16730-1-2015
Fire safety engineering — Procedures and requirements for verification and validation of calculation methods — Part 1: General
消防安全工程 - 计算方法验证和验证的程序和要求 - 第1部分:总则
2015-07-20
GOST R 57700.11-2018
Численное моделирование физических процессов. Процессы ударного взаимодействия. Верификация и валидация численных моделей низкоскоростных ударов и внедрений. Требования
物理过程的数值模拟 影响互动的过程 验证和验证低速碰撞和穿透的数值模型 要求
GOST R 57700.16-2018
Численное моделирование физических процессов. Процессы ударного взаимодействия. Верификация и валидация численных моделей высокоскоростных ударов и внедрений. Общие требования
物理过程的数值模拟 影响互动的过程 验证和验证高速碰撞和穿透的数值模型 一般要求
AAMI/ISO 11607-2-2019
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
最终灭菌医疗器械的包装.第2部分:成型、密封和组装工艺的验证要求
KS P ISO 11607-2
최종 멸균 처리한 의료기기의 포장 — 제2부: 성형, 봉함 및 조립 공정에 대한 유효성 확인 요구사항
终端灭菌医疗器械的包装 - 第2部分:成型 密封和装配过程的验证要求
2018-11-05
KS P ISO 11607-2
최종 멸균 처리한 의료기기의 포장 —제2부: 성형, 봉함 및 조립 공정에 대한 유효성 확인 요구사항
最终灭菌医疗器械的包装.第2部分:成型、密封和装配工艺的验证要求
2021-06-28
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
ISO 11607-2-2019
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
最终灭菌医疗器械包装第2部分:成形 密封和装配过程的验证要求
2019-01-31
YC/T 547.1-2016
烟草行业专用计量器具技术审核规范 第1部分:基本要求和工作程序
Specification of technical check for tobacco special measuring instrument—Part 1:Requirements and procedures
2016-01-23