CAN/CSA-ISO/TS 16775:17
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2 (Adopted ISO technical specification 16775:2014, first edition, 2014-05-15)
Hardcopy , PDF
01-01-2023
English
01-01-2017
Foreword
Introduction
1 Scope
2 Terms and definitions
3 Guidance for health care facilities
4 Guidance for industry
Annex A (informative) - Selection, evaluation
and testing of packaging materials and
sterile barrier systems - Guidance for
industry and health care facilities
Annex B (informative) - Sterilization
considerations - Guidance for industry
and health care facilities
Annex C (informative) - Examples of
wrapping methods - Guidance for health
care facilities
Annex D (informative) - Validation plan
documents - Guidance for health care facilities
Annex E (informative) - Installation qualification
documentation - Guidance for health care facilities
Annex F (informative) - Operational qualification
documentation - Guidance for health care facilities
Annex G (informative) - Performance qualification
documentation - Guidance for health care facilities
Annex H (informative) - Addressing worst-case
requirements - Guidance for industry and health
care facilities
Annex I (informative) - Generating a final packaging
system validation protocol - Guidance for industry
Annex J (informative) - Design inputs - Medical device
attributes - Guidance for industry
Annex K (informative) - Risk analysis tools - Guidance
for industry and health care facilities
Annex L (informative) - Considerations for sampling
plans - Guidance for health care facilities
Annex M (informative) - Stability testing
(ISO 11607-1:2006, 6.4) - Guidance for industry
Annex N (informative) - Use of the Internet - Guidance for
industry and health care facilities
Annex O (informative) - Test method validation -
Guidance for industry
Annex P (informative) - Use of contract packagers -
Guidance for industry and health care facilities
Annex Q (informative) - Guidance on establishing process
parameters - Guidance for industry
Annex R (informative) - Investigation failure -
Guidance for industry and health care facilities
Annex S (informative) - Packaging manufacturing
requirements - Guidance for industry and health
care facilities
Annex I (informative) - Generating a final packaging
system validation protocol - Guidance for industry
Annex J (informative) - Design inputs - Medical device
attributes - Guidance for industry
Annex K (informative) - Risk analysis tools - Guidance
for industry and health care facilities
Annex L (informative) - Considerations for sampling
plans - Guidance for health care facilities
Annex M (informative) - Stability testing
(ISO 11607-1:2006, 6.4) - Guidance for industry
Annex N (informative) - Use of the Internet - Guidance for
industry and health care facilities
Annex O (informative) - Test method validation -
Guidance for industry
Annex P (informative) - Use of contract packagers -
Guidance for industry and health care facilities
Annex Q (informative) - Guidance on establishing process
parameters - Guidance for industry
Annex R (informative) - Investigation failure -
Guidance for industry and health care facilities
Annex S (informative) - Packaging manufacturing
process and packaging system design feasibility
evaluation - Guidance for industry
Bibliography
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