ackages
ackaging material
erformance
hysical testing
ublic health;Qualifications;Quality;Quality assurance;Reuse;Sampling methods;Sealing;Shaping;Specification;Specification (approval);Sterile barrier systems;Sterility;Testing;Validation;Visual inspection (testing)【摘要】: This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.This part of ISO 11607 is applicable to industry, to health care facilities, and wherever medical devices are packaged and sterilized.This part of ISO 11607 does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements may also be necessary for drug/device combinations.【中国标准分类号】: C30【国际标准分类号】: 11_080_30【页数】: 11P;A4【正文语种】: 英语 | 欢迎光临 世界资料网论坛 (http://bbs.infoeach.com/) | Powered by Discuz! X2.5 |