Add to ORKGIn May 2005, the Food and Drug Administration (FDA) issued draft guidance on the type of information to be posted on its new “Drug Watch” website—a site intended to identify drugs for which it is actively evaluating early safety signals. At this time, the FDA plans only to post information on drug products regulated by the Center for Drug Evaluation and Research, therefore vaccines, blood products and medical devices shall be excluded
Study Objective: To review quantitatively and qualitatively the U.S. Food and Drug Administration (F...
This commentary explores the implications of increased social media marketing by drug manufacturers,...
Physician-directed pharmaceutical advertising is regulated in the United States by the Food and Drug...
FDA to Create Drug Safety Board In February 2005, the Food and Drug Administration (FDA) announced t...
On August 15, 2005, the Food and Drug Administration (FDA) and the Association of American Medical C...
This paper seeks (1) to provide the background necessary to understand current commercial speech jur...
Pharmacists in all areas of practice frequently dispense or recommend drugs without realizing that s...
Physicians often prescribe prescription drugs and other medications for uses that are not approved b...
Posted with permission from FDLI ; Food and Drug Law Journal Various proposals have been advanced in...
Background: For the purpose of understanding the Food and Drug Administration’s (FDA’s) concerns reg...
In 1938 the Food and Drug Administration (FDA) adopted regulations which created a category of presc...
The Food and Drug Administration (FDA) is responsible for assuring that drugs, devices, and biologic...
Background: For the purpose of understanding the Food and Drug Administration’s (FDA’s) concerns r...
The regulation off-label drugs is a complicated and controversial area of the law. Regulators must p...
In lieu of an abstract, here is the article\u27s first paragraph: Biotech industry forms the backbon...
Study Objective: To review quantitatively and qualitatively the U.S. Food and Drug Administration (F...
This commentary explores the implications of increased social media marketing by drug manufacturers,...
Physician-directed pharmaceutical advertising is regulated in the United States by the Food and Drug...
FDA to Create Drug Safety Board In February 2005, the Food and Drug Administration (FDA) announced t...
On August 15, 2005, the Food and Drug Administration (FDA) and the Association of American Medical C...
This paper seeks (1) to provide the background necessary to understand current commercial speech jur...
Pharmacists in all areas of practice frequently dispense or recommend drugs without realizing that s...
Physicians often prescribe prescription drugs and other medications for uses that are not approved b...
Posted with permission from FDLI ; Food and Drug Law Journal Various proposals have been advanced in...
Background: For the purpose of understanding the Food and Drug Administration’s (FDA’s) concerns reg...
In 1938 the Food and Drug Administration (FDA) adopted regulations which created a category of presc...
The Food and Drug Administration (FDA) is responsible for assuring that drugs, devices, and biologic...
Background: For the purpose of understanding the Food and Drug Administration’s (FDA’s) concerns r...
The regulation off-label drugs is a complicated and controversial area of the law. Regulators must p...
In lieu of an abstract, here is the article\u27s first paragraph: Biotech industry forms the backbon...
Study Objective: To review quantitatively and qualitatively the U.S. Food and Drug Administration (F...
This commentary explores the implications of increased social media marketing by drug manufacturers,...
Physician-directed pharmaceutical advertising is regulated in the United States by the Food and Drug...