发布时间：2024-05-27 17:49:26 - 更新时间：2024年06月29日 15:22
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本规范适用于新建、扩建和改建的医药工业洁净厂房的设计
Code for design of pharmaceutical industry clean room
现批准《医药工业洁净厂房设计标准》为国家标准，编号为GB50457-2019，自2019年12月1日起实施。其中，第3.2.1、3.2.2、5.1.6、5.1.7、5.1.8、5.1.11、6.4.1、6.4.2、6.4.3、6.4.4、6.4.5、6.4.6、7.2.12、8.2.1
Design standards for clean workshops in the pharmaceutical industry
Cleanroom technology, particle cleanliness classes of the air, Cleanroom technology, Particulate air cleanliness classes
Test methods for suspended particles in clean rooms and clean areas of the pharmaceutical industry
Die Richtlinie beschreibt Erfordernisse an den Betrieb reinraumtechnischer Systeme, die im Rahmen der Qualit?tssicherung spezifiziert werden, um die
Cleanroom technology - Cleanroom operation
This guideline applies to cleanroom clothing intended for repeated use. Single-use cleanroom clothing that is disposed of after use is not the subject
Cleanroom technology - Cleanroom operation - Decontamination of multiple-use cleanroom clothing
The guideline contains the classification of air cleanliness for cleanrooms and associated controlled environments in mathematical, tabular
Cleanroom technology - Particulate air cleanliness classes
Cleanrooms
主要技术内容包括：总则，术语，兽药工业洁净厂房的分级、分类和技术指标，厂区总平面布置，工艺，建筑与装修，结构，空调、通风和净化，给水与排水，动力，电气和生物安全
Design standards for clean workshops in the veterinary drug industry
この規格は，クリーンルーム及びこれに関連する制御された環境(以下，クリーンルーム施設という。)における空気清浄度の浮遊微粒子濃度によるクラス分類及びその評価法について規定する
Classification of air cleanliness for cleanrooms
Part 15 of guideline VDI 2083 covers the requirements for personnel and their clothing in relation to the cleanroom. Furthermore, indications
Cleanroom technology - Personnel at the clean work place
本文件规定了医药工业洁净厂房运行维护技术规范的总则、生产区域、设备、菌药品生产区域、特殊性质药品生产区域、菌室的消毒要求、监测、检测与评价
Technical specification for operation and maintenance of clean workshop in pharmaceutical industry
Cleanliness level and evaluation in clean room (area)
Test methods for clean rooms (areas) of pharmaceutical packaging material production plants
本规范适用于新建、扩建和改建的医药工业洁净厂房的设计
Code for design of pharmaceutical industry clean room
现批准《医药工业洁净厂房设计标准》为国家标准，编号为GB50457-2019，自2019年12月1日起实施。其中，第3.2.1、3.2.2、5.1.6、5.1.7、5.1.8、5.1.11、6.4.1、6.4.2、6.4.3、6.4.4、6.4.5、6.4.6、7.2.12、8.2.1
Design standards for clean workshops in the pharmaceutical industry
Cleanroom technology, particle cleanliness classes of the air, Cleanroom technology, Particulate air cleanliness classes
Test methods for suspended particles in clean rooms and clean areas of the pharmaceutical industry
Die Richtlinie beschreibt Erfordernisse an den Betrieb reinraumtechnischer Systeme, die im Rahmen der Qualit?tssicherung spezifiziert werden, um die
Cleanroom technology - Cleanroom operation
This guideline applies to cleanroom clothing intended for repeated use. Single-use cleanroom clothing that is disposed of after use is not the subject
Cleanroom technology - Cleanroom operation - Decontamination of multiple-use cleanroom clothing
The guideline contains the classification of air cleanliness for cleanrooms and associated controlled environments in mathematical, tabular
Cleanroom technology - Particulate air cleanliness classes
Cleanrooms
主要技术内容包括：总则，术语，兽药工业洁净厂房的分级、分类和技术指标，厂区总平面布置，工艺，建筑与装修，结构，空调、通风和净化，给水与排水，动力，电气和生物安全
Design standards for clean workshops in the veterinary drug industry
この規格は，クリーンルーム及びこれに関連する制御された環境(以下，クリーンルーム施設という。)における空気清浄度の浮遊微粒子濃度によるクラス分類及びその評価法について規定する
Classification of air cleanliness for cleanrooms
Part 15 of guideline VDI 2083 covers the requirements for personnel and their clothing in relation to the cleanroom. Furthermore, indications
Cleanroom technology - Personnel at the clean work place
本文件规定了医药工业洁净厂房运行维护技术规范的总则、生产区域、设备、菌药品生产区域、特殊性质药品生产区域、菌室的消毒要求、监测、检测与评价
Technical specification for operation and maintenance of clean workshop in pharmaceutical industry
Cleanliness level and evaluation in clean room (area)
Test methods for clean rooms (areas) of pharmaceutical packaging material production plants
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