How Is AI Optimizing Different Aspects of FDA Submissions?
The Department of Health and Human Services Regulatory agency is known as The Food and Drug Administration. The FDA is accountable for protecting and promoting public health through controlling and supervising food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, and medical devices. FDA approval is a must for any drug to be on the market. FDA plays a crucial role in reviewing drugs, medical devices, and biologics before it enters the market. The development of pharmaceuticals is a complex and lengthy process. Companies abide by the regulatory body’s guidelines for the effectiveness of the drugs, vaccines, biologics, and medical devices, for which FDA submission is essential and crucial in several steps. Nowadays, companies are leveraging artificial intelligence for effective and quick submissions. The FDA is also developing a new regulatory framework to promote inno