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1. www.fda.gov › regulatory-information › fda-rules-and-regulationsFDA Rules and Regulations

   www.fda.gov › regulatory-information › fda-rules-and-regulations

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   9 kwi 2024 · Federal regulations are either required or authorized by statute. Some, such as FDA’s egg safety regulations, address a specific problem or known health hazard, while others, like citizen ...

2. www.fda.gov › regulatory-informationRegulatory Information | FDA - U.S. Food and Drug Administration

   www.fda.gov › regulatory-information

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   Rules & Regulations. Summary of the FDA's process for rulemaking. Laws Enforced by FDA. The Federal Food, Drug, and Cosmetic Act and other congressional milestones are presented...

3. www.fda.gov › medical-devices › overview-device-regulationCode of Federal Regulations (CFR) | FDA

   www.fda.gov › medical-devices › overview-device-regulation

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   FDA's legal authority to regulate both medical devices and electronic radiation-emitting products is the Federal Food Drug & Cosmetic Act (FD&C Act). The FD&C Act contains provisions,...

4. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug...

   www.accessdata.fda.gov › scripts › cdrh

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   22 mar 2024 · For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). This database includes a codification of the general and permanent rules published in the...

5. www.ecfr.gov › current › title-21eCFR :: Title 21 of the CFR -- Food and Drugs

   www.ecfr.gov › current › title-21

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   Regulations Under Certain Other Acts Administered by the Food and Drug Administration: 1210 – 1299

6. www.ecfr.gov › current › title-21eCFR :: 21 CFR Chapter I -- Food and Drug Administration,...

   www.ecfr.gov › current › title-21

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   Regulations Under Certain Other Acts Administered by the Food and Drug Administration: 1210 – 1299

7. jamanetwork.com › journals › jamaFDA Regulation and Approval of Medical Devices: 1976-2020

   jamanetwork.com › journals › jama

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   Evidence Review Laws enacted by US Congress and regulations promulgated by the FDA through 2020; databases maintained by the FDA of device authorizations from 1976 to 2020; and annual reports of user fees paid to the FDA by industry.