FDA reform

FDA reform refers to updates and changes to how the Food and Drug Administration oversees the safety, effectiveness, and approval of products like medications, medical devices, and food. These reforms aim to streamline approval processes, improve transparency, and ensure timely access to new treatments while maintaining safety standards. They may also enhance oversight of emerging technologies and address current challenges, such as drug pricing or supply chain issues. Overall, FDA reform seeks to balance innovation, public health, and safety to better serve patients and consumers.