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Sterile medical device packaging

When the development and validation of the packaging manufacturing process are completed, the standard testing procedures (e.g., ASTM) should be used to ensure sterile medical device package integrity and the sterility of the product after additional production processes. [Pg.658]

ASTM F 1980-02. 2002. Standard guide for accelerated aging of sterile medical device packages. West Conshohocken, PA American Society for Testing and Materials. [Pg.48]

Standard Guide for Accelerated Aging of Sterile Medical Device Packages, ASTM Standard ASTM F1980-99el, ASTM International, West Conshohocken, PA, 2002. [Pg.60]

See other pages where Sterile medical device packaging is mentioned: [Pg.663]    [Pg.582]    [Pg.584]    [Pg.586]    [Pg.588]    [Pg.590]    [Pg.592]    [Pg.594]    [Pg.595]    [Pg.596]    [Pg.598]    [Pg.599]    [Pg.600]    [Pg.602]    [Pg.604]    [Pg.606]    [Pg.606]    [Pg.608]    [Pg.609]    [Pg.610]    [Pg.611]    [Pg.612]    [Pg.612]    [Pg.614]   
See also in sourсe #XX -- [ Pg.23 ]



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