ISO 11607-2:2019/Amd 1:2023
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management
Section sec_3.29
Section sec_3.30
Section sec_3.31
Annex sec_B
Annex sec_B.1
Annex sec_B.2
Annex sec_B.3
Annex sec_B.3.1
Annex sec_B.3.2
Annex sec_B.4
Table tab_B.1
Annex sec_B.5
Annex sec_B.6
Annex sec_B.7
Annex sec_B.8
Previous versions
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Section sec_3.29
Section sec_3.30
Section sec_3.31
Annex sec_B
Annex sec_B.1
Annex sec_B.2
Annex sec_B.3
Annex sec_B.3.1
Annex sec_B.3.2
Annex sec_B.4
Table tab_B.1
Annex sec_B.5
Annex sec_B.6
Annex sec_B.7
Annex sec_B.8