FDA Modernization Act

The FDA Modernization Act is a U.S. law aimed at improving the efficiency of the Food and Drug Administration (FDA) in reviewing and approving new medicines and treatments. It updates regulations to streamline processes, encourage innovation, and make it easier for companies to bring safe and effective products to market. This act also promotes the use of electronic submissions and emphasizes the importance of patient involvement in drug development, ultimately aiming to enhance public health by ensuring timely access to new therapies.