PDF(1781 KB)
PDF(1781 KB)
PDF(1781 KB)
基于良好审查规范(GRRP)国际协调性指南文件研究对我国医疗器械监管的启示
({{custom_author.role_cn}}), {{javascript:window.custom_author_cn_index++;}}Research and Reflection on the Coordinated Guidelines for Medical Devices Good Regulatory Review Practice Working Group of IMDRF
({{custom_author.role_en}}), {{javascript:window.custom_author_en_index++;}}| {{custom_ref.label}} |
{{custom_citation.content}}
{{custom_citation.annotation}}
|
/
| 〈 |
|
〉 |