CDER Risk Assessment Exercise to Evaluate Potential Risks from the Use of Nanomaterials in Drug Products

被引：12

作者：

Cruz, Celia N. ^{[1
]}

Tyner, Katherine M. ^{[1
]}

Velazquez, Lydia ^{[1
]}

Hyams, Kenneth C. ^{[1
]}

Jacobs, Abigail ^{[1
]}

Shaw, Arthur B. ^{[1
]}

Jiang, Wenlei ^{[1
]}

Lionberger, Robert ^{[1
]}

Hinderling, Peter ^{[1
]}

Kong, Yoon ^{[1
]}

Brown, Paul C. ^{[1
]}

Ghosh, Tapash ^{[1
]}

Strasinger, Caroline ^{[1
]}

Suarez-Sharp, Sandra ^{[1
]}

Henry, Don ^{[1
]}

Van Uitert, Maat ^{[1
]}

Sadrieh, Nakissa ^{[1
]}

Morefield, Elaine ^{[1
]}

机构：

[1] US FDA, Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA

来源：

AAPS JOURNAL | 2013年 / 15卷 / 03期

关键词：

CDER; nanomaterial; nanotechnology; risk assessment; risk management;

D O I：

10.1208/s12248-013-9466-6

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

The Nanotechnology Risk Assessment Working Group in the Center for Drug Evaluation and Research (CDER) within the United States Food and Drug Administration was established to assess the possible impact of nanotechnology on drug products. The group is in the process of performing risk assessment and management exercises. The task of the working group is to identify areas where CDER may need to optimize its review practices and to develop standards to ensure review consistency for drug applications that may involve the application of nanotechnology. The working group already performed risk management exercises evaluating the potential risks from administering nanomaterial active pharmaceutical ingredients (API) or nanomaterial excipients by various routes of administration. This publication outlines the risk assessment and management process used by the working group, using nanomaterial API by the oral route of administration as an example.

引用

页码：623 / 628

页数：6

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