In this one-course specialization, well focus primarily on the documents needed for regulatory approval of drugs by the U.S. Food and Drug Administration. You'll study the format and content requirements of regulatory documents and write excerpts of documents for regulatory submission. You'll learn how to read, interpret and summarize data from clinical trials in various therapeutic areas. Along the way, you'll hone your writing skills for a variety of audiences, including regulatory agencies, medical professionals, patients and the public.