A document that must be submitted by a researcher conducting a clinical trial to examine a new drug or treatment. The investigator consents to conduct the clinical research in accordance with the FDA's Code of Federal Regulations.
What is the FDA?
- In addition to ensuring the security, efficacy, and safety of human and veterinary drugs, biological products and medical devices, the Food and Drug Administration is in charge of safeguarding the public's health by ensuring the security of our country's food supply, cosmetics and radiation-emitting products.
- When a drug is approved by the FDA, it indicates that CDER has analyses the drug's effect data and determined that the drug's known and potential benefits outweigh those risks for the targeted population.
What is the FDA's function?
- The Food and Drug Administration (FDA) is in charge of ensuring the security, safety and efficacy of biological goods, medical devices, our country's food supply, cosmetics and radiation-emitting products in order to safeguard the public's health.
A document that must be submitted by a researcher conducting a clinical trial to examine a new drug or treatment. The investigator consents to conduct the clinical research in accordance with the FDA's Code of Federal Regulations.
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