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  1. 22 de may. de 2024 · The Federal Commission for the Protection against Sanitary Risks (COFEPRIS), the Pharmacopeia of the United Mexican States (FEUM) and the United States of Pharmacopeia (USP) signed today a Memorandum of Understanding which will contribute to the development and strengthening of a bilateral cooperation framework through the ...

  2. 22 de may. de 2024 · COFEPRIS, FEUM y USP fortalecen su cooperación bilateral. La Comisión Federal para la Protección contra Riesgos Sanitarios (COFEPRIS), la Farmacopea de los Estados Unidos Mexicanos (FEUM) y la Farmacopea de los Estados Unidos de América (United States Pharmacopeia, USP por sus siglas en inglés) firmaron hoy un Memorándum de ...

  3. 26 de may. de 2024 · The United States Pharmacopeia (USP) is a pharmacopeia (a compendium of drug information) for the United States published annually by the United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself.

  4. 9 de may. de 2024 · Combines the United States Pharmacopeia (USP) and the National Formulary (NF). The USP-NF contains the pharmacopeial standards for medicines, dosage forms, drug substances, excipients, medical devices, and dietary supplements. You will need to create a free "Access Point" account (using your MCPHS email address) to use USP-NF.

  5. 6 de may. de 2024 · United States Pharmacopeia and the National Formulary (USP-NF) This link opens in a new window

    • Roxanne Bogucka
    • 2016
  6. 20 de may. de 2024 · One key aspect of quality assurance in pharmaceuticals involves strict adherence to microbiological standards set by the United States Pharmacopeia (USP). These standards are crucial for preventing microbial contamination that could compromise patient safety and product integrity.

  7. Hace 6 días · Quality solutions at a glance—navigate quickly through what’s new at USP —our most recently released USP Reference Standards (RS), Pharmaceutical Analytical Impurities (PAIs), and other materials and services around a specific active pharmaceutical ingredient using our Quality Solution Sheets (QSS).