food and drug administration

What are the Regulatory Pathways for Drug Approval?

Before a drug can be approved, it must go through several phases of clinical trials. These trials assess the drug’s safety and efficacy in humans. The FDA reviews the results of these trials to ensure that the benefits of the drug outweigh any potential risks. Toxicological data are crucial in determining appropriate dosage levels and identifying potential side effects.

Frequently asked queries:

What is the FDA's Role in Toxicology?
What is GRAS and How Does it Relate to Toxicology?
What are the Regulatory Pathways for Drug Approval?
How Does the FDA Handle Food Safety?
What is the Role of Post-Market Surveillance?
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What are the Applications of Genetic Testing in Toxicology?
What Are the Long-Term Considerations?
How Can Long-Term Effects of Toxic Exposure be Managed?
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How Can Human Error Be Minimized in Toxicology?
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How to Synthesize Findings from the Literature?
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