CQAF 2017Q3 Meeting Newsletter

On Sept. 11th , 2017, China Quality Assurance Forum (referred to as CQAF) 2017Q3 Meeting was held in Astellas Shanghai and Beijing office. In total 56 members from 53 organizations, including pharmaceutical companies, clinical trial institutions and CROs participated in this conference.

Key topics shared during the meeting were about eConsent, ePRO, and updates of CQAF Projects and CQAF membership registration were introduced as well.

During the meeting, CQAF Chairperson Ms.Heidi Liu recommended members to register in www.cqaf.org to enable access to CQAF resource.

Please refer to Membership webpage for membership benefits and registration guide.

For Website Introduction，please click CQAF website launch_AmyJ_20170911wm.pdf.

GCP Audit Training Program (24-26 Nov, Beijing) GCP Audit Advanced Training Program (27-29 Nov, Beijing) Inspection Management Workshop (6-7 Nov, Beijing)

For more detail regarding eConsent and ePRO, please click page 2.

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2017年9月11日, China Quality Assurance Forum (简称CQAF) 2017年第三季度会议如期在安斯泰来制药上海和北京会议室召开。来自53家包括制药企业、临床试验机构、CRO等56名论坛会员共同参与此会议。

本次会议重点从稽查视角探讨了电子知情同意(eConsent)，电子患者报告结局(ePRO)，同时也更新了CQAF项目和CQAF会员注册流程。

会上，CQAF主席刘海涛女士推荐大家完成www.cqaf.org 网站会员注册，以便获得CQAF资源。会员权益和如何注册，请参见Membership页面

关于网站介绍，请点击CQAF website launch_AmyJ_20170911wm.pdf

临床试验稽查员培训班(初级） (11月24-26日, 北京) 临床试验稽查员培训班（高级） (11月27-29 日, 北京) GCP现场核查-从自查到核查的管理研讨班 (11月6-7 日, 北京)

关于电子知情同意(eConsent)，电子患者报告结局(ePRO)的详细介绍，请点击第二页。