Explore the latest European research news, search for medicines, and read answers to common clinical trial and health care questions. The mission of the European Medicines Agency (EMA) is to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the European Union (EU). The European Medicines Agency is an agency of the European Union in charge of the evaluation and supervision of pharmaceutical products.
The FDA is responsible for ensuring the safety and efficacy (how well they work) of medical products. New treatments go through a thorough review process and are ultimately approved by the FDA before they can be prescribed to the public. Here’s how they do just that. The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation’s food supply, cosmetics, and products that emit radiation.
How much does it cost to bring a new drug or medical product to the public market? Find out here. We’re a science communication and education platform working to improve science literacy and accessibility by fostering the love of science!