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Drug approval

Drug approval is the process by which government agencies, like the U.S. Food and Drug Administration (FDA), evaluate new medications to ensure they are safe and effective for public use. This process typically involves several stages, including laboratory research, animal testing, and multiple phases of human clinical trials. Each stage collects data on the drug's effects, side effects, and optimal dosages. If the results are favorable, the drug receives approval for market use. Post-approval, the drug continues to be monitored for safety, allowing authorities to manage risks and ensure ongoing efficacy.

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    Drug approval is the process by which a new medication is evaluated for safety and effectiveness before it can be sold to the public. This involves several phases of rigorous testing, starting in the lab and moving to clinical trials with volunteers. Regulatory agencies, like the FDA in the U.S., review the results to ensure the drug meets strict standards for quality and safety. If approved, the drug can be marketed, but it continues to be monitored for any long-term effects as it is used by the general population. This process helps protect public health.