GB/T 42168.2-2026 Condoms—Guidance on clinical studies—Part 2:Female condoms,clinical function studies based on self-reports
GB/T 42168.2-2026 Condoms—Guidance on clinical studies—Part 2:Female condoms,clinical function studies based on self-reports
Basic Information
Scope
This document provides guidance on the design, implementation, analysis, and interpretation of clinical trials of female condoms conducted in accordance with the requirements of YY/T 1567.
This document is applicable to comparing the performance of new female condoms with those already on the market during sexual intercourse (not anal intercourse) through clinical trials. The study aims to evaluate acute failure events that occur during use.
This document also provides guidance on data analysis after the completion of the trial, as well as the interpretation of the results by manufacturers and regulatory authorities.
This document does not cover certain issues related to clinical trials, including subject compensation, confidentiality of subjects and their records, and the operation of local ethics committees. Such issues and more detailed guidelines for clinical trial design can be found in YY/T 0297.