
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
Research and Reflection on the Coordinated Guidelines for Medical Devices Good Regulatory Review Practice Working Group of IMDRF
{{custom_ref.label}} |
{{custom_citation.content}}
{{custom_citation.annotation}}
|
/
〈 |
|
〉 |