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马来西亚细胞治疗、组织工程和再生医学产品的临床转化及其监管政策

Clinical Translation of Cell Therapy, Tissue Engineering, and Regenerative Medicine Product in Malaysia and Its Regulatory Policy.

作者信息

Bt Hj Idrus Ruszymah, Abas Arpah, Ab Rahim Fazillahnor, Saim Aminuddin Bin

机构信息

1 Tissue Engineering Centre, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre , Cheras, Kuala Lumpur, Malaysia .

2 Department of Physiology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre , Cheras, Kuala Lumpur, Malaysia .

出版信息

Tissue Eng Part A. 2015 Dec;21(23-24):2812-6. doi: 10.1089/ten.TEA.2014.0521. Epub 2015 Aug 21.

Abstract

With the worldwide growth of cell and tissue therapy (CTT) in treating diseases, the need of a standardized regulatory policy is of paramount concern. Research in CTT in Malaysia has reached stages of clinical trials and commercialization. In Malaysia, the regulation of CTT is under the purview of the National Pharmaceutical Control Bureau (NPCB), Ministry of Health (MOH). NPCB is given the task of regulating CTT, under a new Cell and Gene Therapy Products framework, and the guidelines are currently being formulated. Apart from the laboratory accreditation, researchers are advised to follow Guidelines for Stem Cell Research and Therapy from the Medical Development Division, MOH, published in 2009.

摘要

随着细胞和组织疗法(CTT)在全球范围内用于治疗疾病的不断发展,制定标准化监管政策的需求至关重要。马来西亚的CTT研究已进入临床试验和商业化阶段。在马来西亚,CTT的监管由卫生部(MOH)下属的国家药品监管局(NPCB)负责。根据新的细胞和基因治疗产品框架,NPCB被赋予监管CTT的任务,目前正在制定相关指南。除了实验室认证外,还建议研究人员遵循卫生部医学发展司于2009年发布的《干细胞研究与治疗指南》。

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