The Medicines Act is a piece of legislation that regulates the development, approval, and distribution of medicines and pharmaceutical products. Its primary goal is to ensure that all medicines are safe, effective, and of high quality before they reach the market. This act sets out the requirements for clinical trials, manufacturing practices, and labeling of medicines. Additionally, the Medicines Act establishes a framework for monitoring the safety of medicines after they are approved. It empowers regulatory authorities to take action against any products that pose risks to public health. Overall, the act plays a crucial role in protecting consumers and promoting public health.