WS 324-2010 Abolished Industry standards-Health

WS 324-2010 Standard for human musculoskeletal tissue bank

WS 324-2010 Standard for human musculoskeletal tissue bank

Publish Date: 2010-08-31 Implement Date: 2011-03-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: WS 324-2010
Standard Type: Industry standards
Standard Status: Abolished
is_force_gb: no
CCS Name: Medicine
ICS Name: Integrated medical science and healthcare devices
Publish Date: 2010-08-31
Implement Date: 2011-03-01
Pages: 12 pages

Development Information

Word Count: 18 Thousand words Pages: 12 pages

Referenced Standards

JGJ 71 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/T 19001-2000 Quality management systems—Requirements GB/T 19001-2008 Quality management systems—Requirements GB/T 19001-2016 Quality management systems—Requirements GB/T 19633-2005 Packaging for terminally sterilized medical devices GB/T 19633.1-2015 Packaging for terminally sterilized medical devices—Part 1:Requirements for materials, sterile barrier systems and packaging systems GB/T 19633.1-2024 Packaging for terminally sterilized medical devices—Part 1:Requirements for materials,sterile barrier systems and packaging systems GB/T 19633.2-2015 Packaging for terminally sterilized medical devices—Part 2:Validation requirements for forming,sealing and assembly processes GB/T 19633.2-2024 Packaging for terminally sterilized medical devices—Part 2:Validation requirements for forming,sealing and assembly processes YY/T 0287-2003 Medical devices—Quality management systems—Requirements for regulatory purposes YY/T 0287-2017 Medical devices—Quality management systems—Requirements for regulatory purposes 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

Related Standards

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