兽药GMP洁净区（室）环境检测

T/SICCA 017-2023 洁净室及相关受控环境用夹芯洁净板

本文件规定了洁净室及相关受控环境用夹芯洁净板的原料、技术要求、试验方法、检验规则、标志、标签和随行文件及包装、运输和贮存。 本文件适用于洁净室及相关受控环境用的墙板和吊顶板等夹芯洁净板。 4 原料 4.1 面板 4.2 芯材 4.3 粘结剂

Sandwich panel for cleanroom and associated controlled environments

FCR NAV MIL-HDBK-1028/5 REV A-1994 环境控制 洁净室的设计

ENVIRONMENTAL CONTROL - DESIGN OF CLEAN ROOMS

YY/T 0141-1993 医药工业洁净室和洁净区悬浮粒子的测试方法

YY 0141-1993 医药工业洁净室和洁净区悬浮粒子的测试方法

Test methods for suspended particles in clean rooms and clean areas of the pharmaceutical industry

QJ 2214-1991 洁净室（区）内洁净度级别及评定

Cleanliness level and evaluation in clean room (area)

ASTM E2352-04 航天洁净室和相关受控环境洁净室操作的标准规程

1.1 This practice specifies basic requirements, procedures, and practices for operating aerospace cleanrooms and controlled environments

Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments-Cleanroom Operations

IEST RP-CC046.1-2013 受控环境（航空航天、非洁净室）

Controlled Environments (Aerospace, Non-cleanroom)

VDI 2083 Blatt 12-2000 洁净室技术 安全和环境方面

The document complements Guideline VDI 2083 Part 2 with regard to safty and environmentally relevant measures necessary to control the effects which

Cleanroom technology - Safety and environmental aspects

BS EN ISO 14644-16:2019 洁净室和相关受控环境 洁净室和独立设备的能源效率

What is this ISO 14644 ‑ 16 – Energy efficiency in cleanrooms about? ISO 14644 ‑ 16 is the 16 th part of the multi-series

Cleanrooms and associated controlled environments - Energy efficiency in cleanrooms and separative devices

GB/T 25915.1-2010 洁净室及相关受控环境 第1部分：空气洁净度等级

GB/T 25915的本部分划分洁净室及相关受控环境的空气洁净度等级仅依据其内的空气悬浮粒子浓度,该浓度系指粒径大于或等于阈值(低限)粒径的粒子总数,规定的阈值(低限)粒径为0.1μm～5μm。 本部分未设立0.1μm～5μm 规定粒径以外粒子总数的洁净度等级。但可以用U 描述符和M 描述符

Cleanrooms and associated controlled environments.Part 1:Classification of air cleanliness

UNE 85170:2016 手术室、洁净室和受控环境室的行人门

Pedestrian doors for operating rooms, cleanrooms and controlled environment rooms.

GB/T 16293-1996 医药工业洁净室(区)浮游菌的测试方法

本标准规定了医药工业洁净室和洁净区中浮游菌测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区，菌室或菌区域（包括洁净工作台）的浮游菌的测定和环境的验证

Test method for airborne microbe in clean room (area) of the pharmaceutical industry

GB/T 16294-1996 医药工业洁净室(区)沉降菌的测试方法

本标准规定了医药工业洁净室和洁净区中沉降菌的测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区，菌室或菌区域（包括洁净工作台）的沉降菌的测定与环境的验证

Test method for settling microbe in clean room (area) of the pharmaceutical industry

ASTM E2352-04(2010 航天洁净室和相关受控环境洁净室操作的标准实施规程

1.1 This practice specifies basic requirements, procedures, and practices for operating aerospace cleanrooms and controlled

Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments-Cleanroom Operations

NF EN ISO 14644-2:2016 洁净室和相关受控环境 - 第 2 部分：监测洁净室颗粒空气洁净度性能的维护

Salles propres et environnements maîtrisés apparentés - Partie 2 : surveillance du maintien des performances de la salle propre pour la propreté particulaire de l'air

T/SICCA 017-2023 洁净室及相关受控环境用夹芯洁净板

本文件规定了洁净室及相关受控环境用夹芯洁净板的原料、技术要求、试验方法、检验规则、标志、标签和随行文件及包装、运输和贮存。 本文件适用于洁净室及相关受控环境用的墙板和吊顶板等夹芯洁净板。 4 原料 4.1 面板 4.2 芯材 4.3 粘结剂

Sandwich panel for cleanroom and associated controlled environments

FCR NAV MIL-HDBK-1028/5 REV A-1994 环境控制 洁净室的设计

ENVIRONMENTAL CONTROL - DESIGN OF CLEAN ROOMS

YY/T 0141-1993 医药工业洁净室和洁净区悬浮粒子的测试方法

YY 0141-1993 医药工业洁净室和洁净区悬浮粒子的测试方法

Test methods for suspended particles in clean rooms and clean areas of the pharmaceutical industry

QJ 2214-1991 洁净室（区）内洁净度级别及评定

Cleanliness level and evaluation in clean room (area)

ASTM E2352-04 航天洁净室和相关受控环境洁净室操作的标准规程

1.1 This practice specifies basic requirements, procedures, and practices for operating aerospace cleanrooms and controlled environments

Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments-Cleanroom Operations

IEST RP-CC046.1-2013 受控环境（航空航天、非洁净室）

Controlled Environments (Aerospace, Non-cleanroom)

VDI 2083 Blatt 12-2000 洁净室技术 安全和环境方面

The document complements Guideline VDI 2083 Part 2 with regard to safty and environmentally relevant measures necessary to control the effects which

Cleanroom technology - Safety and environmental aspects

BS EN ISO 14644-16:2019 洁净室和相关受控环境 洁净室和独立设备的能源效率

What is this ISO 14644 ‑ 16 – Energy efficiency in cleanrooms about? ISO 14644 ‑ 16 is the 16 th part of the multi-series

Cleanrooms and associated controlled environments - Energy efficiency in cleanrooms and separative devices

GB/T 25915.1-2010 洁净室及相关受控环境 第1部分：空气洁净度等级

GB/T 25915的本部分划分洁净室及相关受控环境的空气洁净度等级仅依据其内的空气悬浮粒子浓度,该浓度系指粒径大于或等于阈值(低限)粒径的粒子总数,规定的阈值(低限)粒径为0.1μm～5μm。 本部分未设立0.1μm～5μm 规定粒径以外粒子总数的洁净度等级。但可以用U 描述符和M 描述符

Cleanrooms and associated controlled environments.Part 1:Classification of air cleanliness

UNE 85170:2016 手术室、洁净室和受控环境室的行人门

Pedestrian doors for operating rooms, cleanrooms and controlled environment rooms.

GB/T 16293-1996 医药工业洁净室(区)浮游菌的测试方法

本标准规定了医药工业洁净室和洁净区中浮游菌测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区，菌室或菌区域（包括洁净工作台）的浮游菌的测定和环境的验证

Test method for airborne microbe in clean room (area) of the pharmaceutical industry

GB/T 16294-1996 医药工业洁净室(区)沉降菌的测试方法

本标准规定了医药工业洁净室和洁净区中沉降菌的测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区，菌室或菌区域（包括洁净工作台）的沉降菌的测定与环境的验证

Test method for settling microbe in clean room (area) of the pharmaceutical industry

ASTM E2352-04(2010 航天洁净室和相关受控环境洁净室操作的标准实施规程

1.1 This practice specifies basic requirements, procedures, and practices for operating aerospace cleanrooms and controlled

Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments-Cleanroom Operations

NF EN ISO 14644-2:2016 洁净室和相关受控环境 - 第 2 部分：监测洁净室颗粒空气洁净度性能的维护

Salles propres et environnements maîtrisés apparentés - Partie 2 : surveillance du maintien des performances de la salle propre pour la propreté particulaire de l'air