FDA Announces New Prescription Drug Information Format to Improve Patient Safety
Rockville, MD: Food and Drug Administration, 2006 January 18; 3p. [Online]. Accessed: http://www.fda.gov/bbs/topics/news/2005/NEW01272.html [2007 April 26]
Showing items related by title, author, creator and subject.
Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products and Draft Guidances and Two Guidances for Industry on the Content and Format of Labeling for Human Prescription Drug and Biological Products; Final Rule and Notices Unknown author (United States. Food and Drug Administration [FDA], 2006-01-24)
A Bill to Amend the Federal Food, Drug and Cosmetic Act to Provide for a Federal Drug Compendium Which Provides Reliable, Complete, and Readily Accessible Prescribing Information; to Assure Safety and Efficacy of Drugs Through Certification Of Certain Drugs Other Than Insulin and Antibiotics; to Require Certain Information in Drug Labeling; and to Improve the Administration and Enforcement of the Act as It Relates to Drugs Unknown author (United States. Congress. Senate, 1979)