T/SZCA 2-2021 Active Group standards

T/SZCA 2-2021 Sanitary production workshop environment online monitoring technical specification

T/SZCA 2-2021 Sanitary production workshop environment online monitoring technical specification

Publish Date: 2021-03-27 Implement Date: 2021-06-19 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us
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Basic Information

Standard Code: T/SZCA 2-2021
Standard Type: Group standards
Standard Status: Active
is_force_gb: no
CCS Name: Health
ICS Name: Information technology applications
Publish Date: 2021-03-27
Implement Date: 2021-06-19
Pages: 40 pages

Scope

1.0.1 In order to standardize the monitoring and management of the environment in clean production workshops, build a space environment that meets the production standards for clean products, grasp the environmental indicator parameters of the production workshops in real time, and reduce operational risks, these regulations are hereby formulated.
1.0.2 These regulations are applicable to environmental monitoring in clean production spaces, such as those in the food, chemical, and general electronics industries; the production spaces in the precision electronics and pharmaceutical industries can refer to these regulations for implementation; these regulations are not applicable to the production environments involving flammable and explosive products.
1.0.3 The environmental safety monitoring of clean production workshops should target the overall production workshop's destruction mode, and promptly feedback on the problems found during the safety monitoring.
1.0.4 Before installing monitoring instruments and equipment, they should be tested and calibrated, and the measuring instruments should be regularly verified and calibrated.
1.0.5 The environmental monitoring of clean production workshops should achieve data display and safety status reporting in offline, online, and cloud-based forms.
1.0.6 In addition to complying with these regulations, the environmental monitoring of clean production workshops should also comply with the provisions of the relevant national standards currently in force.

Development Information

Word Count: 46 Thousand words Pages: 40 pages

Referenced Standards

GB/T 16292-1996 Test method for airborne particles in clean room (area) the pharmaceutical industry GB/T 16292-2010 Test method for airborne particles in clean room (zone) of the pharmaceutical industry GB/T 16293-1996 Test method for airborne microbe in clean room(area) the pharmaceutical industry GB/T 16293-2010 Test method for airborne microbe in clean room(zone) of the pharmaceutical industry GB/T 16294-1996 Test method for settling microbe in clean room(area) the pharmaceutical industry GB/T 16294-2010 Test method for settling microbe in clean room(zone) of the pharmaceutical industry GB 19489-2004 Laboratories—General requirements for biosafety GB 19489-2008 Laboratories—General requirements for biosafety GB/T 20988-2007 Information security technology—Disaster recovery specifications for information systems GB/T 29765-2013 Information security technology—Technical requirements and testing and evaluating method for data backup and recovery products GB/T 29765-2021 Information security technology—Technical requirements and testing and evaluating approaches for data backup and recovery products GB 50073-2013 Code for design of clean room GB 50457-2019 Standard for design of pharmaceutical industry clean room 《药品生产质量管理规范(2010年修订)》 GB/T 20988-2025 Cybersecurity technology—Disaster recovery specifications for information systems GB 50472-2008 Code for design of electronic industry clean room GB 50591-2010 Code for construction and acceptance of cleanroom GB 50687-2011 Architectural and technical code for cleanroom in food industry GB/T 16292-2025 Test method for airborne particles in clean room(zone) of the pharmaceutical industry GB/T 16293-2025 Test method for airborne microbe in clean room(zone) of the pharmaceutical industy GB/T 16294-2025 Test method for settling microbe in clean room (zone)of the pharmaceutical industy

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