Guidance for industry, FDA staff, and FDA-accredited third parties Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA) [[electronic resource]]

• Pubblicazione: [Rockville, Md.] : , : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health; [Bethesda, Md.] : , : Center for Biologics Evaluation and Research, , [2009]
• Descrizione fisica: 1 online resource (10 pages)
• Soggetto topico: Medical instruments and apparatus - Government policy - United States
• Note generali: Title from PDF title screen (viewed May 24, 2012).; "Document issued on March 2, 2009."; "This document supercedes the document which was issued on September 15, 2005."
• Altri titoli varianti: Guidance for industry, Food and Drug Administration staff, and Food and Drug Administration accredited third parties.; Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)
• Titolo autorizzato: Guidance for industry, FDA staff, and FDA-accredited third parties
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910697175103321
• Lo trovi qui: Univ. Federico II