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An Act to Amend the Federal Food, Drug, and Cosmetic Act to Revise and Extend the User-Fee Programs for Prescription Drugs, Medical Devices, Generic Drugs, and Biosimilar Biological Products, and for Other Purposes
An Act to Amend the Federal Food, Drug, and Cosmetic Act to Revise and Extend the User-Fee Programs for Prescription Drugs, Medical Devices, Generic Drugs, and Biosimilar Biological Products, and for Other Purposes
Pubbl/distr/stampa [Washington, D.C.] : , : [U.S. Government Publishing Office], , 2017
Descrizione fisica 1 online resource (86 unnumbered pages)
Soggetto topico Drugs - Prices - Law and legislation - United States
Prescription pricing - Law and legislation - United States
Medical instruments and apparatus industry - Law and legislation - United States
Generic drugs - Prices - United States
Biologicals - Law and legislation - United States
User charges - Law and legislation - United States
Soggetto genere / forma Statutes and codes.
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910706512203321
[Washington, D.C.] : , : [U.S. Government Publishing Office], , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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An Act to Repeal an Unnecessary Medical Device Reporting Requirement
An Act to Repeal an Unnecessary Medical Device Reporting Requirement
Pubbl/distr/stampa [Washington, D.C.] : , : [U.S. Government Printing Office], , [1996]
Descrizione fisica 1 online resource (1 unnumbered leaf)
Soggetto topico Cardiac pacemaker industry - Law and legislation - United States
Medical instruments and apparatus industry - Law and legislation - United States
Soggetto genere / forma Statutes and codes.
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910708698103321
[Washington, D.C.] : , : [U.S. Government Printing Office], , [1996]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee and Modernization Act reauthorization, drug safety, and certain pediatric pharmaceutical and device legislation [[electronic resource] ] : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, June 12, 2007
Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee and Modernization Act reauthorization, drug safety, and certain pediatric pharmaceutical and device legislation [[electronic resource] ] : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, June 12, 2007
Pubbl/distr/stampa Washington : , : U.S. G.P.O., , 2008
Descrizione fisica vi, 311 pages : digital, PDF file
Soggetto topico Prescription pricing - Law and legislation - United States
Medical instruments and apparatus industry - Law and legislation - United States
Pediatric pharmacology - United States
Drugs - Safety measures - Government policy - United States
User charges - Law and legislation - United States
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Discussion drafts concerning Prescription Drug User Fee Act reauthorization, Medical Device User Fee and Modernization Act reauthorization, drug safety, and certain pediatric pharmaceutical and device legislation
Record Nr. UNINA-9910697826103321
Washington : , : U.S. G.P.O., , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Examining FDA's Medical Device User Fee Program : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session, March 28, 2017
Examining FDA's Medical Device User Fee Program : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Fifteenth Congress, first session, March 28, 2017
Pubbl/distr/stampa Washington : , : U.S. Government Publishing Office, , 2018
Descrizione fisica 1 online resource (iii, 107 pages) : illustrations
Soggetto topico User charges - Law and legislation - United States
Medical instruments and apparatus industry - Law and legislation - United States
Soggetto genere / forma Legislative hearings.
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Examining FDA's Medical Device User Fee Program
Record Nr. UNINA-9910711658403321
Washington : , : U.S. Government Publishing Office, , 2018
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The FDA and worldwide quality system requirements guidebook for medical devices / / compiled and written by Amiram Daniel & Ed Kimmelman
The FDA and worldwide quality system requirements guidebook for medical devices / / compiled and written by Amiram Daniel & Ed Kimmelman
Autore Daniel Amiram
Edizione [Second edition.]
Pubbl/distr/stampa Milwaukee, Wisconsin : , : ASQ Quality Press, , 2008
Descrizione fisica 1 online resource (334 p.)
Disciplina 344.7304/2
Altri autori (Persone) TrautmanKimberly A. <1964->
Soggetto topico Medical instruments and apparatus industry - Law and legislation - United States
Quality control - Law and legislation - United States
Medical instruments and apparatus industry - United States - Quality control
Medical instruments and apparatus industry - Law and legislation
Quality control - Law and legislation
Medical instruments and apparatus industry - Quality control
ISBN 0-87389-203-8
0-87389-204-6
600-00-4861-0
1-62198-206-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910789476403321
Daniel Amiram  
Milwaukee, Wisconsin : , : ASQ Quality Press, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The FDA and worldwide quality system requirements guidebook for medical devices / / compiled and written by Amiram Daniel & Ed Kimmelman
The FDA and worldwide quality system requirements guidebook for medical devices / / compiled and written by Amiram Daniel & Ed Kimmelman
Autore Daniel Amiram
Edizione [Second edition.]
Pubbl/distr/stampa Milwaukee, Wisconsin : , : ASQ Quality Press, , 2008
Descrizione fisica 1 online resource (334 p.)
Disciplina 344.7304/2
Altri autori (Persone) TrautmanKimberly A. <1964->
Soggetto topico Medical instruments and apparatus industry - Law and legislation - United States
Quality control - Law and legislation - United States
Medical instruments and apparatus industry - United States - Quality control
Medical instruments and apparatus industry - Law and legislation
Quality control - Law and legislation
Medical instruments and apparatus industry - Quality control
ISBN 0-87389-203-8
0-87389-204-6
600-00-4861-0
1-62198-206-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910817373103321
Daniel Amiram  
Milwaukee, Wisconsin : , : ASQ Quality Press, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The FDA and worldwide quality system requirements guidebook for medical devices / / compiled and written by Amiram Daniel & Ed Kimmelman
The FDA and worldwide quality system requirements guidebook for medical devices / / compiled and written by Amiram Daniel & Ed Kimmelman
Edizione [Second edition.]
Pubbl/distr/stampa Milwaukee, Wisconsin : , : ASQ Quality Press, , 2008
Descrizione fisica 1 online resource (334 p.)
Disciplina 344.7304/2
Altri autori (Persone) TrautmanKimberly A. <1964->
Soggetto topico Medical instruments and apparatus industry - Law and legislation - United States
Quality control - Law and legislation - United States
Medical instruments and apparatus industry - United States - Quality control
Medical instruments and apparatus industry - Law and legislation
Quality control - Law and legislation
Medical instruments and apparatus industry - Quality control
Soggetto genere / forma Electronic books.
ISBN 600-00-4861-0
1-62198-206-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910464166503321
Milwaukee, Wisconsin : , : ASQ Quality Press, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Journal of GXP compliance
Journal of GXP compliance
Pubbl/distr/stampa Royal Palm Beach, FL, : Institute of Validation Technology
Disciplina 353.9/97/097305
Soggetto topico Pharmacy - Law and legislation - United States
Medical instruments and apparatus industry - Law and legislation - United States
Food law and legislation - United States
Pharmaceutical Preparations - standards
Clinical Trials as Topic - standards
Drug and Narcotic Control - legislation & jurisprudence
Equipment and Supplies - standards
Quality Control
Food law and legislation
Medical instruments and apparatus industry - Law and legislation
Pharmacy - Law and legislation
Soggetto genere / forma Periodical
Periodicals.
ISSN 2150-6590
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti GXP compliance
Record Nr. UNISA-996209185003316
Royal Palm Beach, FL, : Institute of Validation Technology
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Reauthorization of MDUFA : what it means for jobs, innovation, and patients : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, second session, February 15, 2012
Reauthorization of MDUFA : what it means for jobs, innovation, and patients : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Twelfth Congress, second session, February 15, 2012
Pubbl/distr/stampa Washington : , : U.S. Government Printing Office, , 2012
Descrizione fisica 1 online resource (iv, 224 pages) : illustrations
Soggetto topico Medical instruments and apparatus industry - Law and legislation - United States
User charges - Law and legislation - United States
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Reauthorization of MDUFA
Record Nr. UNINA-9910704344303321
Washington : , : U.S. Government Printing Office, , 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Reauthorization of the Medical Device User Fee and Modernization Act [[electronic resource] ] : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 16, 2007
Reauthorization of the Medical Device User Fee and Modernization Act [[electronic resource] ] : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Tenth Congress, first session, May 16, 2007
Pubbl/distr/stampa Washington : , : U.S. G.P.O., , 2008
Descrizione fisica v, 150 pages : digital, PDF file
Soggetto topico Medical instruments and apparatus industry - Law and legislation - United States
User charges - Law and legislation - United States
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Reauthorization of the Medical Device User Fee and Modernization Act
Record Nr. UNINA-9910697742703321
Washington : , : U.S. G.P.O., , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui