1) Exhibit Evaluation
展品评审
3) EMEA
欧盟药品审评局
1.
According to USA FDA,and EU EC,EMEA,and FVO related regulations,this paper introduced the basic registration requirements of Chinese Traditional Medicine to apply marketing authorization in USA and EU.
参阅美国食品药品监督管理局(FDA,Food and Drug Administration);欧盟委员会(EC,European Commis-sion);欧盟药品审评局(EMEA,The European Agency for the Evaluation of Medicinal Products)及欧盟食品兽医办公室(FVO,Food and Veterinary Office)有关法律法规文件,就中药在欧美国家申请上市注册的基本要求做简要介绍。
4) product quality review
产品质量评审
6) aesthetic evaluation for the artwork
作品审美评价
补充资料：展品
1.即展览品。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条