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Learn about the history and current status of cannabis legalization in Maryland, including medical and recreational use, decriminalization, and expungement. Find out the details of the 2022 referendum that legalized recreational cannabis and the related laws and regulations.
CBER is one of six main centers for the U.S. Food and Drug Administration (FDA), responsible for assuring the safety, purity, potency, and effectiveness of biologics and related products. Learn about CBER's history, scope, authority, and activities, such as vaccine regulation and adverse event reporting.
CDER is a division of the U.S. Food and Drug Administration that monitors and reviews drugs and biological products. It has eight sections with different responsibilities, such as clinical trials, generic drugs, post-marketing surveillance, and policy development.
The FDA is a federal agency of the US Department of Health and Human Services that regulates various products and activities related to public health. It enforces the Federal Food, Drug, and Cosmetic Act and other laws, and has 14 centers and offices across the country.
The U.S. Food and Drug Administration is holding a two-day public hearing to start the process of creating an abbreviated approval procedure for so-called biosimilar and interchangeable biological ...
CMC stands for chemistry, manufacturing, and control, a part of drug development that involves testing and optimizing the properties and production of a new chemical entity (NCE). NCE is a compound that emerges from drug discovery and enters preclinical and clinical trials to become a new drug.
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