關於「FDA」標籤，搜尋引擎有相關的訊息討論：

FDA食藥登錄平台 - 衛生福利部食品藥物管理署。

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GL Holdings Issues Voluntary Worldwide Recall of Green Lumber ...。

2019年10月22日 · When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service.。

AccessGUDID (for the public) | FDA。

2018年3月23日 · The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical ...： tw | tw。

How US FDA's GRAS Notification Program Works。

2018年2月9日 · Within FDA, the Center for Food Safety and Applied Nutrition's (CFSAN) Office of Food Additive Safety is responsible for reviewing safety ...： tw | tw。

Regulations: Good Clinical Practice and Clinical Trials | FDA。

Links to FDA's clinical trial,human subject protection, informed consent regulations and preambles.： 。

510(k) Premarket Notification - US Food and Drug Administration。

Super Search Devices@FDA 6 ... 510(k) Number, K981351. Device Name, CANDELA GENTLELASE GL DERMATOLOGICAL LASER. Applicant ...。

FDA approves first oral GLP-1 treatment for type 2 diabetes。

2019年9月20日 · FDA approves Rybelsus (semaglutide) oral tablets to improve blood sugar in adults with type 2 diabetes, with diet and exercise.： 。

Establishment Registration & Device Listing - Accessdata.fda.gov。

2021年10月11日 · ... SUNRISE-RC/ST GENALYSER; SUNRISE-RC/ST GL.ABBOTT; SUNRISE-RC/ST ML; SUNRISE-RC/ST RMP; SUNRISE-RC/ST TC CRE; SUNRISE-RC/TW EVOLYZER 29 ...。

FDA approves Inflectra, a biosimilar to Remicade。

2016年4月5日 · The U.S. Food and Drug Administration today approved Inflectra (infliximab-dyyb) for multiple indications. Inflectra is administered by ...。

Food & Drug Administration | HHS.gov。

The Food and Drug Administration (FDA) is an HHS agency that regulates clinical investigations of products under its jurisdiction, such as drugs, ...