YY/T 1998-2026 Pending Industry standards-Medicine

YY/T 1998-2026 General requirements for clinical investigation of in vitro diagnostic reagents

Publish Date: 2026-03-09 Implement Date: 2027-03-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1998-2026

Standard Type: Industry standards

Standard Status: Pending

is_force_gb: no

CCS Name: Medical devices

ICS Name: Medical equipment

Publish Date: 2026-03-09

Implement Date: 2027-03-01

Publisher: 国家药品监督管理局

Technical Committee: 全国医疗器械临床评价标准化技术归口单位

Pages: 24 pages

Scope

本文件规定了对体外诊断（IVD）试剂的临床性能和安全性进行评估而实施的临床试验全过程的质量通用要求，包括临床试验计划、方案设计、实施、监查、稽查、检查以及数据的采集、记录、保存、分析、总结和报告等。
本文件适用于以注册为目的的体外诊断试剂临床试验。

Development Information

Drafting Units:

国家药品监督管理局医疗器械技术审评中心、国家药品监督管理局食品药品审核查验中心

Drafting Persons:

吕允凤、何静云、李冉、李晓丽、王佳楠、燕娟

Word Count: 35 Thousand words Pages: 24 pages

Referenced Standards

YY/T 1956-2025 Clinical investigation of in vitro diagnostic reagents—Terms and definitions

Related Standards

GB 9706.8-1995 Replaced

GB 9706.8-1995 Medical electrical equipment—Part 2:Particular requirements for the safety of cardiac defibrillators and cardiac defibrillator-monitors

Publish Date: 1995-06-02

GB 11235-1997 Replaced

GB 11235-1997 VCu intra-uterine device

Publish Date: 1997-07-24

GB/T 17257.1-1998 Replaced

GB/T 17257.1-1998 Urine collection bags—Part 1:Vocabulary

Publish Date: 1998-03-18

GB/T 17257.2-1998 Replaced

GB/T 17257.2-1998 Urine collection bags—Part 2:Determination of dimensions

Publish Date: 1998-03-18

GB/T 17257.3-1998 Replaced

GB/T 17257.3-1998 Urine collection bags—Part 3:Verification of rated volume

Publish Date: 1998-03-18

GB/T 17257.4-1998 Replaced

GB/T 17257.4-1998 Urine collection bags—Part 4:Determination of freedom form leakage

Publish Date: 1998-03-18