Assuring quality and performance of sustained and controlled release parenterals: Workshop report

AAPS PharmSci Pub Date : 2008-01-01 DOI:10.1208/ps040205
D. Burgess, A. Hussain, T. Ingallinera, Mei-ling Chen
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引用次数: 89

Abstract

This is a summary report of the American Association of Pharmaceutical Scientists, the Food and Drug Administration and the United States Pharmacopoeia cosponsored workshop on “Assuring Quality and Performance of Sustained and Controlled Release Parenterals.” Experts from the pharmaceutical industry, the regulatory authorities and academia participated in this workshop to review, discuss and debate formulation, processing and manufacture of sustained and controlled release parenterals and identify critical process parameters and their control. Areas were identified where research is needed in order to understand the performance of these drug delivery systems and to assist in the development of appropriate testing procedures. Recommendations were made for future workshops, meetings and working groups in this area.
确保持续控释注射剂的质量和性能:车间报告
这是美国药物科学家协会、食品和药物管理局和美国药典共同主办的关于“确保缓控释注射剂的质量和性能”研讨会的总结报告。来自制药业、监管部门和学术界的专家参加了本次研讨会,对缓释注射剂的配方、加工和生产进行了审查、讨论和辩论,并确定了关键工艺参数及其控制。确定了需要进行研究的领域,以便了解这些给药系统的性能,并协助制定适当的检测程序。为今后这方面的讲习班、会议和工作组提出了建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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