The Food and Drug Administration (FDA) reviews manufacturers or processors of FDA-regulated products to ensure that they comply with relevant regulations.
The FDA is the body that oversees the organization's core functions related to medical and tobacco products, food and veterinary medicine, global regulatory operations, and policy and operations. You may know more about US FDA inspection 483.
The FDA review process takes into account the protection of public health by ensuring that food is safe, healthy, hygienic, and properly labeled, thereby ensuring that pharmaceuticals, vaccines, and other organic and medical devices are safe and for use by humans and animals. effective.
The FDA process also considers protecting electronic products from emissions, ensuring cosmetics and food additives are safe and properly labeled, regulates tobacco products, and improves public health by helping accelerate product innovation. The FDA reviews manufacturers or processors of FDA-regulated products to ensure that they comply with applicable regulations.
The FDA's review process also includes vaccine and drug manufacturers, blood banks, food processors, dairy farms, feed processors, and pharmacies, excluding facilities that conduct clinical studies on imported human and animal products.
Topics and observations to be covered during the FDA include processing equipment, employee practices, food storage / exposure, water and drainage, and pest control.
Due to the fact that all FDA regulated facilities are undoubtedly subject to FDA, it is imperative that staff receive regular training on what to expect and what role they should play during the FDA process.