Reference number
ISO 29943-1:2017
International Standard
ISO 29943-1:2017
Condoms — Guidance on clinical studies — Part 1: Male condoms, clinical function studies based on self-reports
Edition 1
2017-07
Read sample
ISO 29943-1:2017
62497
Published (Edition 1, 2017)
This publication was last reviewed and confirmed in 2023. Therefore this version remains current.

ISO 29943-1:2017

ISO 29943-1:2017
62497
Language
Format
CHF 173
Convert Swiss francs (CHF) to your currency

Abstract

ISO 29943-1:2017 is intended to help in the design, execution, analysis and interpretation of clinical function studies conducted in accordance with the requirements of ISO 23409 for male synthetic condoms.

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

ISO 29943-1:2017 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.

General information

  •  : Published
     : 2017-07
    : International Standard confirmed [90.93]
  •  : 1
     : 42
  • ISO/TC 157
    11.200 
  • RSS updates

Sustainable Development Goals

This standard contributes to the following Sustainable Development Goal

Got a question?

Check out our Help and Support