The new drugs still requireFood and Drug Administrationapproval before they will be widely aailable. 这两种新药在大规模上市之前须获食品与药物管理局的批准. 互联网 展开全部 英英释义 Noun 1. a federal agency in the Department of Health and Human Services established to regulate the release of new...
Although it was not known by its present name until 1930, FDA’s modern regulatory functions began with the passage of the 1906 Pure Food and Drugs Act, a law a quarter-century in the making that prohibited interstate ...
FDA- Food and Drugs Administration Food and Drug Administration Divers/Alimentation et nutrition FDA- Failure to Do Anything Ne rien faire. Divers/Non classé FDA- Freedom to Do Anything La liberté de faire quoi que ce soit Divers/Non classé ...
Although it was not known by its present name until 1930, FDA’s modern regulatory functions began with the passage of the 1906 Pure Food and Drugs Act, a law a quarter-century in the making that prohibited interstate commerce in adulterated and misbranded food and drugs. Harvey Washington W...
On new drugs development, two Clinical Trial Licenses (藥物臨床試驗批件) have been obtained fromtheState Food and Drug Administration(SFDA), PRC. legco.gov.hk legco.gov.hk 在開發新藥物方面,中藥研究院從中國國家食品藥品監督管理局取得兩份藥物臨牀試驗批件。
It was not until 1906 that the first federal Pure Food and Drug Act was enacted, which made it a federal crime to sell mislabeled or adulterated food, drink, and drugs intended for interstate commerce. This cornerstone legislation of the future Food and Drug Administration was passed following ...
Food and Drug Administration- a federal agency in the Department of Health and Human Services established to regulate the release of new foods and health-related products FDA Department of Health and Human Services,Health and Human Services,HHS- the United States federal department that administers ...
Understanding the Food and Drug Administration (FDA) The Food and Drug Administration is the federal government agency assigned to protect and promote public health. This is done by assessing and assuring "the safety, efficacy, and security of human and veterinary drugs, biological products, medical...
The Food and Drug Administration is a federal agency responsible for ()laws designed to protect purity and safety of food and drugs. A.enforcingB.enhancingC.endowingD.entailing 相关知识点: 试题来源: 解析 A 题意是:食品和药品管理局是一个负责___为保护食品和药物的洁净和安全而制定的法律的...
Imported foods must be pure, wholesome, safe to eat, and produced under sanitary conditions; drugs and devices must be safe and effective; cosmetics must be safe and made from approved ingredients; radiation-emitting devices must meet established standards; and all products must contain informative ...