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I find it very troubling that students are asking people on Answers.com to do their homework for them. There are many who ask health related questions. The failure to study and understand the material to be able to answer these questions will put patients at risk.
Who wants an intellectually lazy doctor, nurse, pharmacist or other health professional making decisions about their life ?
What else can I help you with?
Which regulatory agency would initiate a class II recall on a prescription drug?
The FDA
Is the food and drug administration owned by the government?
The Food and Drug Administration (FDA) is a regulatory agency of the United States Federal Government, so in a sense, yes it is owned by them.
What are not functions by FDA?
In the context of the FDA, "not functions" typically refer to products or substances that do not meet the regulatory definition of a drug, biologic, or medical device. This can include items like dietary supplements, cosmetics, or food products that are not intended for therapeutic use. Additionally, certain claims made about products may lead to them being classified as not functions if they don't align with FDA definitions. Products that do not undergo the necessary approval processes or fail to demonstrate safety and efficacy may also fall into this category.
What is FDA drug rating?
what is FDA drug rating
When was the USFDA created?
Although it was not known as the FDA until 1930, the regulatory functions began with the passage of the 1906 Pure Food and Drugs Act.
What is the cost from drug company to the fda for a new drug?
The cost for a drug company to develop a new drug and gain FDA approval can range from hundreds of millions to over a billion dollars. This figure includes expenses for research and development, clinical trials, regulatory fees, and other associated costs. The FDA charges specific fees for services such as New Drug Application (NDA) submissions, which can amount to several million dollars. Overall, the financial burden reflects the lengthy and complex process required to bring a new drug to market.
What does the drug FDA stand for?
Food and Drug Administration ( pharmacy Terminology)
What is the full form of fda?
The full form of FDA is the Food and Drug Administration. It is a regulatory agency of the United States Department of Health and Human Services, responsible for protecting public health by ensuring the safety, efficacy, and security of drugs, medical devices, and food products.
Is the FDA an independent regulatory agency?
What is the primary purpose of a health care regulatory agency.
What is russia fda?
The term "Russia FDA" typically refers to the Federal Service for Surveillance in Healthcare, known as Roszdravnadzor, which is the regulatory body overseeing the safety and efficacy of medicines and medical devices in Russia. It functions similarly to the U.S. Food and Drug Administration (FDA), ensuring that health products meet specific standards before being approved for use. Roszdravnadzor also monitors compliance with health regulations and conducts inspections of healthcare facilities and pharmaceutical companies.
The letter D in the letters FDA stands for the word?
it stands for "drug" as in medicines....Food & Drug Administration
What does acronym fDa stands for what?
FDA means Food and Drug Administration.
