Food And Drug Administration ( Fda ) - 871 Words

According to the US Food and Drug Administration (FDA), the definition of a drug includes the following; â€Å"a substance recognized by an official pharmacopoeia or formulary. A substance intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease. A substance (other than food) intended to affect the structure or any function of the body. A substance intended for use as a component of a medicine, but not a device or a component, part or accessory of a device. Biological products are included within this definition and are generally covered by the same laws and regulations, but differences exist regarding their manufacturing processes (chemical process versus biological process)† (F.D.A. 2012). Making medications safe, efficacious and affordable have been a long lime pursuit by the US government, pharmaceutical industries and advocacy groups and ordinary citizens of the US. This responsibility started with regulations of vaccines in early 19th century by the government. At the time infectious disease was a major killer in the whole world and vaccines have been proven to be effective in combating infectious. However, the techniques and standards available today were not available then but some sort of regulation still needed to be put in place to ensure safety. After over a century following the vaccines act, some progress was made as regards drug policies and making medication safer amongst which includes the pure food and drug act of 1906 which isShow MoreRelatedSupplements : Dietary Supplements, As Defined By The Fda ( U.s. Food And Drug Administration1344 Words   |  6 PagesIETARY SUPPLEMENTS Dietary supplements, as defined by the FDA (U.S. Food and Drug Administration), are products intended for ingestion which contain any ingredients which add further nutritional value to the diet. Dietary supplements fall under the food category and consist vitamins, minerals, herbs, amino acids, metabolites, extracts (U.S. Food and Drug and Administration (FDA), 2015). Supplements are taken by many people to assist in the building of muscle and to assist in recovery after workoutsRead MoreThe Lack Of Regulation From The Food And Drug Administration ( Fda ) On Electronic Cigarette Products2292 Words   |  10 PagesThe lack of regulation from the Food and Drug Administration (FDA) on electronic cigarette products is creating a desire for state and local governments to enact laws aimed to address their usage (Balakit, 2014). In Maryland, House Bill 0026, Clean Indoor Air Act – Use of Electronic Smoking Devices – Prohibition, was intended to make the use of electronic cig arettes (e-cigarettes), â€Å"battery-operated devices that contain nicotine cartridges and other chemicals,† illegal in public places (SubramaniamRead MoreSafety Of Food And Drugs Consumption1448 Words   |  6 PagesSafety in food and drugs consumption is a necessity to consumers. It is the FDA s responsibility to ensure food and drug safety for the public. That’s why the FDA is what happens when agency within the U.S. Department of Health and Human Services (HHS) responsible for ensuring the safety and effectiveness. As the Food and Drug Administration Progresses it had became a reliable source for Americans .President Theodore Roosevelt signed the Food, Drug, and Cosmetic Act in 1938 to provide the publicRead MoreRegulatory Agency Paper1549 Words   |  7 Pages Federal Drug and Food Administration â€Å"The Federal Drug Administration is an agency within the Department of Health and Human Services. The FDA organization consist of the Office of Commissioner and four directorates overseeing four core functions of the agency: Medical Products, and Tobacco, Foods, Global Regulatory Operations, and Policy, and Operations† (FDA, 2011). The FDA is responsible ensuring the safety of the public by makingRead MoreRegulatory Agency: Food and Drug Administration Essay1617 Words   |  7 PagesAgency: Food and Drug Administration Victoria Steele University of Phoenix Regulatory Agency: Food and Drug Administration The regulation of all areas of health care in The United States falls to The United States Department of Health and Human. One such area is the regulation on medications dispensed within the United States. The section of The United States Department of Health and Human Services responsible for regulation on medications is the Food and Drug Administration (FDA). WhereasRead MoreShould Drugs Be Safe For Consumption?1688 Words   |  7 Pagesthese medications will benefit your health? How do you know that the drugs are safe for you? Every day, men and women enter hospitals because of a doctor’s appointment or because of an infirmity. Most of them will have prescribed drugs from doctors, but none of them will question of the effectiveness and safety of the pharmaceuticals. There are also many other ways to obtain drugs like through a local drug store, but the drugs are considered to be safe for consumption. This is because the UnitedRead MoreThe Food and Drug Adminstratio n Essay1384 Words   |  6 PagesThe Food and Drug Administration Over the last one hundred and eighty years, The United States has had numerous kinds of, chemist, doctors, politicians and concerns citizens that came together to form different types of groups and agencies to oversee consumer products and meet minimal guidelines. Over the decades the guidelines have become stricter with emphasis on intense processing and regulations on consumer products. During these early years, there were no federal agencies to protectRead MoreFood And Drug Administration V Brown Williamson940 Words   |  4 PagesFood Drug Administration v. Brown Williamson 529 U.S. 120 (2000) Parties: 1) Petitioner- Food Drug Administration 2) Respondent- Brown Williamson Tobacco Corporation Facts: The Food and Drug Administration issued a rule in 1996 that prohibited the tobacco products labeling, promotion, and availability to young people (children and adolescents). The FDA claimed that as per Food, Drug, and Cosmetic Act (FDCA), it had authority to regulate tobacco products because nicotineRead MoreFood And Drug Act Of 19061565 Words   |  7 PagesEveryday you consume things may it be food, drinks, or prescription drugs. Most people will just absent mindedly intake these products subconsciously knowing that they are monitored by government organizations ensuring your safety. It has not always been that was and has progressed greatly throughout the years. although all consumer safety organizations may not be reputable, they do much more good than harm. Consumer safety is something that is extremely important to the American family, and hasRead MoreFood Safety And Security : Usda And Fda1530 Words   |  7 PagesFood Safety and Security: USDA and FDA Abstract The USDA and FDA have been resources for the United States of America to turn to in regards to policies and procedures dealing with food safety and security. In this report you will find the histories of the USDA and FDA, how humans, animals and the environment are benefited by these organizations and new policies that the USDA and FDA have released recently. Historical Background †¢ Up until the mid-1800’s people s main concern when it