论文部分内容阅读
2005年10.1-2006年9.30 3FDA目标3——通过更好的制造和产品监督来提高产品的质量、安全和可获取性为了确保医疗器械和辐射性器械的安全和有效,CDRH制定和颁布了良好制造规范要求;对上市产品监控其顺应性和监督项目;对产品的不良效果报告
2005 2006 - 2006 9.30 3FDA Goal 3 - Improve product quality, safety and accessibility through better manufacturing and product monitoring In order to ensure the safety and effectiveness of medical and radiological equipment, the CDRH has developed and promulgated the Good Manufacturing specifications requirements; monitoring of compliance with listed products and supervision of the project; the adverse effects of the product report