Active standard | Published: 06/07/2017

ISO 29943-2:2017

Condoms — Guidance on clinical studies — Part 2: Female condoms, clinical function studies based on self-reports
(Préservatifs — Lignes directrices relatives aux études cliniques — Partie 2: Préservatifs féminins, analyse fonctionnelle des défaillances graves sur la base d´auto-déclarations)

Available languages: English

Available design: electronic design (pdf), Print design

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Detail information

Designation: ISO 29943-2:2017

Publication date: 06/07/2017

Pages: 40

Country: International technical standard

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Anotation

Description / Abstract: 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.

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