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ISO 29943-2:2017

Current

Current

The latest, up-to-date edition.

Condoms — Guidance on clinical studies — Part 2: Female condoms, clinical function studies based on self-reports

Available format(s)

Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users

Language(s)

English

Published date

06-07-2017

€165.00
Excluding VAT

ISO 29943-2:2017 is intended to help in the design, execution, analysis, and interpretation of clinical function studies conducted in accordance with the requirements of ISO 25841 for female condoms.

These clinical studies compare the performance of a new female condom to an established female condom during vaginal intercourse (not anal intercourse). In particular, these studies are designed to assess acute failure events during use.

ISO 29943-2:2017 also provides direction on the analysis of data when the study is completed, as well as interpretation of these results by manufacturers and regulatory bodies.

Certain clinical trial elements are not addressed in this document, including compensation, confidentiality of individuals and their records, use of local ethics committees, etc. These and many other clinical trial design issues are covered in greater detail in ISO 14155.

Committee
ISO/TC 157
DevelopmentNote
Supersedes ISO/DIS 29943-2. (07/2017)
DocumentType
Standard
Pages
40
PublisherName
International Organization for Standardization
Status
Current

Standards Relationship
IS/ISO 29943 : Part 2 : 2017 Identical
BS ISO 29943-2:2017 Identical
NEN ISO 29943-2 : 2017 Identical

BS ISO 25841:2017 Female condoms. Requirements and test methods
ISO 25841:2017 Female condoms — Requirements and test methods

ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
ISO 25841:2017 Female condoms — Requirements and test methods
ISO 16037:2002 Rubber condoms for clinical trials Measurement of physical properties
ISO 14155:2011 Clinical investigation of medical devices for human subjects Good clinical practice
ISO 14971:2007 Medical devices Application of risk management to medical devices

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