首页

Welcome to CQAF

The China QA Forum (CQAF) was set up in May 2010 and is a Leading Quality Assurance Platform in China aiming to promote GxP Quality Standards in the Healthcare Industry.

For more, click About CQAF

Meeting

1 .2026.05.31 | CLQA 2026 Q2 Meeting

2 .Inviting you to CQAF 2024 Q2 Meeting

MORE >

Training

1 .General Principles of Records and Information Mgmt

2 .Quality Mgmt in China GCP institution

MORE >

Publications

1 .从CRC现况看研究者团队的真实履职

2 .临床试验研究中心选择

MORE >

Newsletters

1 .“New to Quality” 第五期——聚焦流程管理，夯实临床试验质量体系执行根基

2 .“New to Quality” 第四期——供应商管理

MORE >

News

1 .让质量"看得见、可对话"——CAR如何重塑药物研发质量管理新范式

2 .当AI进入临床研究，谁对AI的判断负责？ | CQAF AI for Auditing Vol. 2

MORE >

Regulatory Express

1 .Regulatory Express_July 2026

2 .Regulatory Express_Apr. 2026

MORE >

Mentor/Mentee

1 .Regulatory Express_July 2026

2 .Regulatory Express_Apr. 2026

MORE >

Buddy Coach

1 .Regulatory Express_July 2026

2 .Regulatory Express_Apr. 2026

MORE >

News

View all

“New to Quality” 第五期——聚焦流程管理，夯实临床试验质量体系执行根基
2026-07-13 00:46:27

2026年3月27日，“New to Quality”项目第五期培训正式开展。本期聚焦“流程管理”主题，由Maria Jin、王靖华两位导师联合主讲，围绕临床试验流程管理框架、实施方法与落地要求进行了全面系统的讲解。
Regulatory Express_July 2026
2026-07-13 00:44:43

The International Council for Harmonization (ICH) has announced the adoption of Annex 2 to the guideline on Good Clinical Practices (GCPs) E6(R3). This annex focuses on the collection of data from a wider range of sources for clinical trials, including decentralized trials and pragmatic clinical trials (PCTs). The finalized version of Annex 2 does not include any major changes from the draft guideline issued in November 2024.
“New to Quality” 第四期——供应商管理
2026-07-09 20:54:40

2026年3月6日，New to Quality项目第四期课程“GCP供应商稽查”如期开讲。本期课程由颜旭老师主讲，作为第三期“供应商管理”主题的深度延续，聚焦于GCP供应商稽查从策划到执行的全流程实践，为学员系统梳理了稽查落地的关键环节与操作要点。

Useful Link

Regulatory Authority

Industry Association