Article 3 The State Food and Drug Administration shall take charge of the work of supervision over and administration of pharmaceutical production nationwide.
第三条国家食品药品监督管理局主管全国药品生产监督管理工作；
Article 3 the State Food and Drug administration shall be in charge of the work of supervision and administration on the licensing of national pharmaceutical trading.
第三条国家食品药品监督管理局主管全国药品经营许可的监督管理工作。
In 2005 the State Drug Administration should be invited to participate in the conference final GMP pharmaceutical excipients and medicinal material management practices seminars;
2005年应国家药品监督管理局邀请，参与了药用辅料GMP定稿工作会议和药用辅料管理办法的讨论会；
Article 3 Pharmaceutical directions and labels shall be subject to the ratification of the State Food and Drug Administration.
第三条药品说明书和标签由国家食品药品监督管理局予以核准。
Article 3 Pharmaceutical directions and labels shall be subject to the ratification of the State Food and Drug Administration.
第三条药品说明书和标签由国家食品药品监督管理局予以核准。
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