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  3. www.fda.gov › medical-devices › device-registration-andSearch Registration and Listing | FDA

    Releasable establishment registration and listing information under the Freedom of Information Act is available by searching the Establishment Registration and Listing database. The database is ...

  4. www.fda.gov › food › cfsan-constituent-updatesFDA Releases Report on Economically Motivated Adulteration ...

    2024年4月8日 · April 8, 2024. The U.S Food & Drug Administration (FDA) is releasing data from a sampling assignment carried out in 2022 and 2023 to test imported honey for economically motivated adulteration ...

  5. 香港六合彩熱搜 - Yahoo搜尋結果

  6. www.fda.gov › safety › medwatch-fda-safety-information-andMedical Product Safety Information | FDA

    2022年11月9日 · Safety Alerts for Human Medical Products (Drugs, Biologics, Medical Devices, Special Nutritional Products and Cosmetics) MedWatch alerts provide timely new safety information on human drugs ...

  7. www.fda.gov › drugs › pharmaceutical-quality-resourcesCurrent Good Manufacturing Practice (CGMP) Regulations | FDA

    2023年5月19日 · The CGMP regulations for drugs contain minimum requirements for the methods, facilities, and controls used in manufacturing, processing, and packing of a drug product. The regulations make sure ...

  8. www.fda.gov › medical-devices › cdrh-international-affairsMedical Device Single Audit Program (MDSAP) | FDA

    2023年9月19日 · The Medical Device Single Audit Program allows an MDSAP recognized Auditing Organization to conduct a single regulatory audit of a medical device manufacturer that satisfies the relevant ...

  9. www.fda.gov › regulatory-information › search-fda-guidanceCPG Sec 555.425 Foods, Adulteration Involving hard or Sharp ...

    CPG Sec 555.425 Foods, Adulteration Involving hard or Sharp Foreign Objects. BACKGROUND: Hard or sharp foreign objects in food may cause traumatic injury including laceration and perforation of ...

  10. www.fda.gov › medical-devices › quality-system-qs-regulationQuality Management System Regulation: Final Rule Amending ...

    2024年1月31日 · On January 31, 2024, the FDA issued a final rule amending the device current good manufacturing practice (CGMP) requirements of the Quality System (QS) Regulation under 21 CFR 820 to align more ...

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