US FDA Registration

What is U.S FDA ? The Food and Drug Administration (FDA or USFDA) is a federal agency which is the part of the United States Department of Health and Human Services. It is one of the United States federal executive departments. The FDA evaluates and approves many different things, including: · new drugs, including biologics, · food additives for people and animals, · color additives in food, drugs, and cosmetics for people and animals, · some medical devices The U.S. Food and Drug Administration (FDA) is responsible for regulating medical devices used to diagnose, prevent and treat COVID-19, such as diagnostic tests, ventilators, and personal protective equipment (PPE) including surgical masks, face shields, respirators, gowns, and gloves. Personal Protective Equipment (PPE): Respirators, Surgical Masks, Gowns, Gloves, and More Personal protective equipment (PPE) refers to protective clothing, helmets, gloves, face shields, goggles, surgical masks, respirators, and other equipment designed to protect the wearer from injury or help prevent wearer exposure to infection or illness. PPE is commonly used in health care settings such as hospitals, doctor's offices, and clinical labs, as well as veterinary hospitals, food production facilities, and food service settings. When used properly, PPE acts as a barrier between infectious materials (such as viral and bacterial contaminants) and your skin, mouth, nose, or eyes (mucous membranes). The barrier provided by the PPE has the potential to block transmission of contaminants from blood, body fluids, or respiratory secretions when used properly. PPE may also protect patients who are at high risk for contracting infections through a surgical procedure or who have a medical condition, such as an immunodeficiency, from being exposed to substances or potentially infectious material brought in by visitors and health care workers.