Last updated on October 15th, 2024 at 06:33 pm
In many countries, generic drugs must be approved by the appropriate regulatory agency before they can be sold to the public. These regulatory agencies are responsible for evaluating the safety, efficacy, and quality of all medications, including generic drugs, and ensuring that they meet the necessary standards.
Overall, the process for approving generic drugs is designed to ensure that they are safe and effective for use, and that they meet the same standards as brand-name drugs.
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