“The US Food and Drug Administration is tasked with granting marketing approval to manufacturers that wish to sell prescription drugs and medical devices to the public. Many people are interested in the pace of new drug approvals, but for CME writers this assumes special importance. Numerous CME projects arise from the need for physicians and other healthcare providers to learn about the mechanisms of action and side effect profiles of newly approved drugs. ”
Excerpt from: CME Writer's Marketplace, 2020 Edition
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