The Pure Food and Drug Act’s main aim was to inform consumers of the existence of certain substances in food that was available for general purchase. The substances specifically named in the Pure Food and Drug Act included alcohol, morphine, opium, cocaine, heroin, and cannabis as at the t...
The future role of pharmacologists in the evaluation of drugs will increase as scientific knowledge and our understanding of drugs and disease processes increase. In addition, political issues and public fears will place further demands on the scientific community to try to influence the drug ...
In the past, the Food and Drug Administration (FDA) was criticized for delays in the approval of potentially life-saving drugs; this criticism led to efforts to expedite the drug-approval process. However, the studies used to obtain product approval typically involve limited patient populations, ...
加拿大:根据加拿大的《食品和药品法》(The Food and Drug Act),包括中药在内的自然健康产品不是食品就应算作药品,自… blog.sina.com.cn|基于14个网页 2. 食品与药品法 因为在加拿大实行的《食品与药品法》(The Food and Drug Act)的附表中没有中药这一栏目,而加拿大的药典中也没有中药这 … ...
The article examines the implications upon drug safety and health-system pharmacies as a result of the implementation of the U.S. Food and Drug Administration Amendments Act (FDAAA) of 2007. The author asserts that the FDAAA enhanced the authority of the FDA during postmarketing ...
The Food and Drug Administration (FDA) is announcing a publication containing modifications the Agency is making to the list of standards FDA recognizes for use in premarket reviews (FDA recognized consensus standards). This publication, entitled ‘‘Modifications to the List of Recognized Standards, ...
An amendment, known as the "Moore" amendment, has been proposed to modify the Federal Food, Drug and Cosmetic Act. If it is enacted, proof of wilful intent or gross negligence would be required before a criminal conviction for violation of the Federal Food, Drug and Cosmetic Act could be ...
The FDA Safety and Innovation Act. The authors discuss the impact of the U.S. Food and Drug Administration (FDA) Safety and Innovation Act for the review of prescription drugs and medical de... Steinbrook,Robert - 《Jama Journal of the American Medical Association》 被引量: 11发表: 2012年...
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With the passage of the Food and Drug Administration Modernization Act (FDAMA), existing programs for expedited development and approval for treatments of serious or life-threatening diseases were codified and consolidated under the administrative rubric of fast track product designation. The four basic...