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FDA OVERSIGHT HEARING ON CODEX BADLY NEEDED 7 wrmd - fda

FDA OVERSIGHT HEARING ON CODEX BADLY NEEDED 7 wrmd - fda 2025

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The document is a letter addressed to Congressman Dan Burton, urging him to hold a hearing regarding the FDA's handling of Codex comments on vitamins and minerals. It criticizes the FDA for ignoring congressional requests and for using an unscientific risk assessment model that contradicts established safety data on dietary supplements. The author calls for the withdrawal of certain FDA comments and emphasizes the need for adherence to existing laws protecting dietary supplement regulations.

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What has the FDA been wrong about?

Allegations that unsafe drugs are approved Some critics believe that the FDA has been apt to overlook safety concerns in approving new drugs, and is slow to withdraw approved drugs once evidence shows them to be unsafe.

What has the FDA failed to do?

The FDA Often Fails to Demand Sufficient Clinical Evidence of Claims. While the FDA does not necessarily control every word on the packaging of a drug, it certainly has the power to stop improper pharmaceutical marketing.

What are some issues the FDA deals with?

The committee identified four major vulnerabilities in the U.S. drug safety system: (1) chronic underfunding; (2) organization problems, particularly inadequate integration of pre-and postmarket data review; (3) a range of technical problems related to the insufficient quantity and quality of postmarket data and

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