ECA新闻20150512：ECA和PQG公布EU GDP第6章解读
2015-05-13
12/05/2015
ECA and PQG publish Chapter 6 of the interpretation ofthe EU GDP Guideline
ECA和PQG公布EU GDP第6章解读
The ECA Foundation and thePharmaceutical Quality Group (PQG) have been working on the interpretation ofdifferent chapters of the EU GDP Guideline. The interpretation of five chaptershave been published already. The following 5 Guidance chapters on the EU GDP Guideline are available: ECA组织和药品质量组（PQG）经着手在制订EU GDP指南不同章节的诠释。以下五章的解读已经公布：
Chapter 1: Quality Management
Chapter 9: Transportation (also contains a template for a Technical Agreement)
Chapter 7: Outsourced Activities
Chapter 2: Personnel
Chapter 5: Operations
第1章：质量管理
第9章：运输（还包括技术协议的模板）
第7章：外包活动
第2章：人员
第5章：运营
Now the group has finalized the work onchapter 6 - Complaints, Returns, Suspected Falsified Medicinal Products &Medicinal Product Recalls. Chapter 6 of the EU GDP Guideline requires thatall complaints, returns, suspected falsified medicinal products and recallsmust be recorded and handled carefully according to written procedures. Somereturned medicinal products might be released for resale. The handling shouldbe performed only after an assessment of the returned medicinal products. Theapproval should be made by the Responsible Person (RP). Also complaints must behandled based on a written procedure and all details of each complaint mustbe recorded. Finally, the identification and handling of Falisified MedicinalProducts are also defined in chapter 6. The ECA/PQG Guidance document providesinformation on how to implement the requirements.
现在药品质量组已经完成了对第6章—投诉、退货、疑似假药和医疗产品召回的解读制订工作。EU GDP指南的第6章要求所有投诉、退货、疑似假药和召回必须根据书面程序进行记录和处理。有些退回的药品可以再次放行销售。只有在对退回的药品进行评估后才可以进行处理。必须由负责人（RP）进行批准。投诉也必须根据书面程序进行处理，每个投诉的所有细节都必须记录。最后，假药的辨识和处理也在第6章进行了定义。ECA/PQG指南文件提供了如何实施这些要求的信息。
你可以在GDP工作组上述网址会员区找到GDP指南的第6章和其它章节。会员免费。