drug approval

What role do regulatory agencies play in drug approval?

Regulatory agencies like the [FDA](https://www.fda.gov), the European Medicines Agency (EMA), and other national bodies are responsible for reviewing and approving new cancer treatments. They evaluate the data from preclinical and clinical studies to ensure the drug is safe and effective for patients. These agencies also monitor post-market safety to identify any long-term or rare side effects that may arise after the drug is widely used.

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