BS EN 16602-70-58:2015 - Space product assurance. Bioburden control of cleanrooms

BS EN 16602-70-58:2015

Space product assurance. Bioburden control of cleanrooms

Status : Current   Published : September 2015

Format
PDF

Format
HARDCOPY



This standard establishes the principles and basic methodology for microbiological control of cleanrooms and associated controlled environments with planetary protection constraints. This standard does not address: • the microbiological contamination control of spaceflight hardware; • molecular contamination control. Reference is made to other documents; • fire and safety regulations; for these, see regulatory requirements and other national or local documentation. This standard does not lay down the methods for determining the microbiological and particulate cleanliness levels. Reference is made to other documents. This standard may be tailored for the specific characteristic and constrains of a space project in conformance with ECSS-S-ST-00.




Standard NumberBS EN 16602-70-58:2015
TitleSpace product assurance. Bioburden control of cleanrooms
StatusCurrent
Publication Date30 September 2015
Normative References(Required to achieve compliance to this standard)EN 16601-00-01, ECSS-S-ST-00-01, EN 16602-10-09, ECSS-Q-ST-10-09, EN 16602-20, ECSS-Q-ST-20, EN 16602-20-07, ECSS-Q-ST-20-07, EN 16602-70-55, ECSS-Q-ST-70-55, ISO 14644 part 1:1999, ISO 14644 part 2:2000
Informative References(Provided for Information)EN 16601-00, ECSS-S-ST-00, ISO 14698 part 1, ISO 14698 part 2, IEST-RP-CC023.2, ASTM D1193
International RelationshipsEN 16602-70-58:2015
DescriptorsSpace technology, Space transport, Aerospace transport, Air transport, Quality assurance, Quality control, Production management, Production planning, Product design, Design, Consumer-supplier relations, Quality management, Project management
ICS49.140
Title in FrenchAssurance produit des projets spatiaux. Contrôle de la charge microbienne des salles blanches
Title in GermanRaumfahrtproduktsicherung. Kontrolle der Gesamtkeimzahl in Reinräumen
CommitteeACE/68
ISBN978 0 580 86590 9
PublisherBSI
FormatA4
DeliveryYes
Pages48
File Size1.234 MB
Price£240.00


 Your basket
Your basket is empty

Multi-user access to over 3,500 medical device standards, regulations, expert commentaries and other documents


Develop a PAS

Develop a fast-track standardization document in 9-12 months


BSOL

The faster, easier way to work with standards


Tracked Changes

Understand the changes made to a standard with our new Tracked Changes version