2025年11月21日 · The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and …...
2026年3月24日 · The listing of FD&C Act sections presented here identifies both the FD&C Act and U.S. Code section numbers, which can be used to narrow your search on the Law Revision Counsel website....
2023年10月31日 · FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other notifications. FIS ha...
2026年4月13日 · FD&C Act Chapter V: Drugs and Devices ... To search the FD&C Act on the Law Revision Counsel website, you may either search by U.S. code section number or browse the Title 21 …...
2026年3月24日 · The table below provides a convenient way to search for FDA guidance documents from a single location. You can search for documents using key words, and you can narrow or filter …...
2025年12月7日 · To determine if your product meets the definition of a medical device, you should define the intended use and indications for use of your product. Once you have defined the intended …...
2024年11月21日 · To search the FD&C Act on the Law Revision Counsel website, you may either search by U.S. code section number or browse the Title 21 section listing.
Update: February 2, 2026 The Quality Management System Regulation (QMSR) that became effective on February 2, 2026, amends the device current good manufacturing practice (CGMP) requirements …
2026年3月25日 · Earlier this year, FDA revoked the authorization for FD&C Red No. 3. “Parents and doctors have concerns about petroleum-based food dyes, which have no nutritional benefit,” said …...
2024年12月24日 · For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).