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The American Board of Toxicology is the oldest and largest certification body in the world to ensure the competency of toxicologists involved in preclinical drug discovery. [5] Board certification is available to a licensed attorney in the United States as well, although it generally is not considered a form of licensure and usually does not ...
The regulation of drug advertising in the U.S. is divided between the Food and Drug Administration (FDA) and the Federal Trade Commission (FTC), based on whether the drug in question is a prescription drug or an over-the-counter (OTC) drug. The FDA oversees the advertising of prescription drugs, while the FTC regulates the advertising of OTC drugs.
Medical device (such as hearing aids, for example) may be specified by a type of prescription. Off-label use – Use of pharmaceuticals for conditions different from that for which they were approved. Prescription analytics. Prescription charges – Charges for medical prescriptions on the UK NHS, and in Ireland.
www.usmle.org. The United States Medical Licensing Examination (USMLE) is a three-step examination program for medical licensure in the United States sponsored by the Federation of State Medical Boards (FSMB) and the National Board of Medical Examiners (NBME). [9] Physicians with a Doctor of Medicine (MD) degree are required to pass the USMLE ...
Law. Category. v. t. e. A medical license is an occupational license that permits a person to legally practice medicine. In most countries, a person must have a medical license bestowed either by a specified government-approved professional association or a government agency before they can practice medicine.
The regulation of therapeutic goods, defined as drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as in Australia.
A drug policy is the policy regarding the control and regulation of psychoactive substances (commonly referred to as drugs), particularly those that are addictive or cause physical and mental dependence. While drug policies are generally implemented by governments, entities at all levels (from international organisations, national or local ...
The United States Pharmacopeia (USP) is a pharmacopeia (compendium of drug information) for the United States published annually by the over 200-year old United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself.