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The textbook of pharmaceutical medicine [[electronic resource] /] / edited by John P. Griffin, John Posner, Geoffrey R. Barker
The textbook of pharmaceutical medicine [[electronic resource] /] / edited by John P. Griffin, John Posner, Geoffrey R. Barker
Edizione [7th ed.]
Pubbl/distr/stampa Chichester, West Sussex [U.K.], : Wiley-Blackwell, : BMJ Books, 2013
Descrizione fisica 1 online resource (855 p.)
Disciplina 615.1
Altri autori (Persone) GriffinJ. P (John Parry)
PosnerJohn
BarkerGeoffrey R
Soggetto topico Drug approval
Pharmacology
Clinical trials
ISBN 1-118-53235-X
1-118-53233-3
1-299-40273-9
1-118-53234-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Research and development -- pt. 2. Regulation -- pt. 3. Health care marketplace.
Record Nr. UNINA-9910139037503321
Chichester, West Sussex [U.K.], : Wiley-Blackwell, : BMJ Books, 2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The textbook of pharmaceutical medicine / / edited by John P. Griffin, John Posner, Geoffrey R. Barker
The textbook of pharmaceutical medicine / / edited by John P. Griffin, John Posner, Geoffrey R. Barker
Edizione [7th ed.]
Pubbl/distr/stampa Chichester, West Sussex [U.K.], : Wiley-Blackwell, : BMJ Books, 2013
Descrizione fisica 1 online resource (855 p.)
Disciplina 615.1
Altri autori (Persone) GriffinJ. P (John Parry)
PosnerJohn
BarkerGeoffrey R
Soggetto topico Drug approval
Pharmacology
Clinical trials
ISBN 1-118-53235-X
1-118-53233-3
1-299-40273-9
1-118-53234-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Research and development -- pt. 2. Regulation -- pt. 3. Health care marketplace.
Record Nr. UNINA-9910813127103321
Chichester, West Sussex [U.K.], : Wiley-Blackwell, : BMJ Books, 2013
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The textbook of pharmaceutical medicine [[electronic resource] /] / edited by John P. Griffin and John O'Grady
The textbook of pharmaceutical medicine [[electronic resource] /] / edited by John P. Griffin and John O'Grady
Edizione [5th ed.]
Pubbl/distr/stampa Oxford ; ; Malden, Mass., : Blackwell, c2006
Descrizione fisica x, 870 p. : ill
Disciplina 615/.1
Altri autori (Persone) GriffinJ. P (John Parry)
O'GradyJohn, Professor
Soggetto topico Pharmacology, Experimental
ISBN 0-470-98726-X
0-470-98739-1
9786611319991
1-281-31999-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Development of medicines : full development / Alan G. Davies and Peter D. Stonier -- The medical department / Darrall L. Higson with revisions by Peter D. Stonier -- Medical marketing / John H. Young -- Information and promotion / D. Michael Humphreys -- The supply of unlicensed medicines for particular patient use / Amanda Wearing and John O'Grady -- Legal and ethical issues relating to medicinal products / Christine H. Bendall, Christopher J.S. Hodges -- The safety of medicines / A. Peter Fletcher and Susan Shaw -- History of drug regulation in the United Kingdom / John P. Griffin and Rashmi R. Shah -- Regulation of human medicinal products in the European Union / Rashmi R. Shah and John P. Griffin --
Discovery of new medicines / Anand S. Dutta -- Pharmaceutical development / Gavin Halbert -- Preclinical safety testing / David J. Tweats -- Exploratory development / John Posner -- Clinical pharmacokinetics / Paul Rolan and Valeria Molnar -- Purpose and design of clinical trials / Roger A. Yates -- Conduct of clinical trials : good clinical practice / Roger A. Yates -- Medical statistics / Andrew P. Grieve --
European regulation of medicinal devices / Christopher J.S. Hodges -- Technical requirements for registration of pharmaceuticals for human use : the ICH process / Dean W.G. Harron -- The regulation of drug products by the United States food and drug administration -- Peter Barton Hutt -- The US FDA in the drug development, evaluation and approval process / Richard N. Spivey, Judith K. Jones, William Wardell and William Vodra -- Past evolution and future prospects of the Pharma Industry and its regulation in the USA / William Wardell, William Vodra, Judith K. Jones and Richard N. Spivey -- Regulatory and clinical trial approval systems in Japan / Yuichi Kubo -- The regulation of therapeutic products in Australia / Janice Hirshorn and Deborah Monk -- Economics of healthcare / Carole Bradley and Jane R. Griffin -- Controls on NHS medicines prescribing and expenditure in the UK (an historical perspective) with some international comparisons / John P. Griffin and Jane R. Griffin.
Record Nr. UNINA-9910796078503321
Oxford ; ; Malden, Mass., : Blackwell, c2006
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The textbook of pharmaceutical medicine [[electronic resource] /] / edited by John P. Griffin and John O'Grady
The textbook of pharmaceutical medicine [[electronic resource] /] / edited by John P. Griffin and John O'Grady
Edizione [5th ed.]
Pubbl/distr/stampa Oxford ; ; Malden, Mass., : Blackwell, c2006
Descrizione fisica x, 870 p. : ill
Disciplina 615/.1
Altri autori (Persone) GriffinJ. P (John Parry)
O'GradyJohn, Professor
Soggetto topico Pharmacology, Experimental
ISBN 0-470-98726-X
0-470-98739-1
9786611319991
1-281-31999-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Development of medicines : full development / Alan G. Davies and Peter D. Stonier -- The medical department / Darrall L. Higson with revisions by Peter D. Stonier -- Medical marketing / John H. Young -- Information and promotion / D. Michael Humphreys -- The supply of unlicensed medicines for particular patient use / Amanda Wearing and John O'Grady -- Legal and ethical issues relating to medicinal products / Christine H. Bendall, Christopher J.S. Hodges -- The safety of medicines / A. Peter Fletcher and Susan Shaw -- History of drug regulation in the United Kingdom / John P. Griffin and Rashmi R. Shah -- Regulation of human medicinal products in the European Union / Rashmi R. Shah and John P. Griffin --
Discovery of new medicines / Anand S. Dutta -- Pharmaceutical development / Gavin Halbert -- Preclinical safety testing / David J. Tweats -- Exploratory development / John Posner -- Clinical pharmacokinetics / Paul Rolan and Valeria Molnar -- Purpose and design of clinical trials / Roger A. Yates -- Conduct of clinical trials : good clinical practice / Roger A. Yates -- Medical statistics / Andrew P. Grieve --
European regulation of medicinal devices / Christopher J.S. Hodges -- Technical requirements for registration of pharmaceuticals for human use : the ICH process / Dean W.G. Harron -- The regulation of drug products by the United States food and drug administration -- Peter Barton Hutt -- The US FDA in the drug development, evaluation and approval process / Richard N. Spivey, Judith K. Jones, William Wardell and William Vodra -- Past evolution and future prospects of the Pharma Industry and its regulation in the USA / William Wardell, William Vodra, Judith K. Jones and Richard N. Spivey -- Regulatory and clinical trial approval systems in Japan / Yuichi Kubo -- The regulation of therapeutic products in Australia / Janice Hirshorn and Deborah Monk -- Economics of healthcare / Carole Bradley and Jane R. Griffin -- Controls on NHS medicines prescribing and expenditure in the UK (an historical perspective) with some international comparisons / John P. Griffin and Jane R. Griffin.
Record Nr. UNINA-9910814644603321
Oxford ; ; Malden, Mass., : Blackwell, c2006
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The textbook of pharmaceutical medicine [[electronic resource]]
The textbook of pharmaceutical medicine [[electronic resource]]
Edizione [4th ed. /]
Pubbl/distr/stampa London, : BMJ Books, 2002
Descrizione fisica 1 online resource (896 p.)
Disciplina 615.1
Altri autori (Persone) GriffinJ. P (John Parry)
O'GradyJohn
Soggetto topico Pharmaceutical chemistry
Pharmacology
Soggetto genere / forma Electronic books.
ISBN 1-280-19787-0
9786610197873
1-4051-4606-0
1-4237-1777-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Contents; Contributors; Preface; Acknowledgements; The editors; 1: Discovery of new medicines; 2: Pharmaceutical development; 3: Toxicity testing; 4: Exploratory development; 5: Clinical pharmacokinetics; 6: Clinical trials and good clinical practice; 7: Medical statistics; 8: Development of medicines: full development; 9: The medical department; 10: Medical marketing; 11: Information and promotion; 12: The supply of unlicensed medicines for particular patient use; 13: Legal and ethical issues relating to medicinal products; 14: The safety of medicines
15: The development of the control of human medicines in Europe from classical times to the year 200016: Technical requirements for registration of pharmaceuticals for human use: the ICH process and the common technical document; 17: The regulation of drug products by the United States Food and Drug Administration; 18: The US FDA in the drug development, evaluation and approval process; 19: Regulatory and clinical trial systems in Japan; 20: Economics of healthcare; 21: Controls on NHS medicines prescribing and expenditure in the UK (a historical perspective); Appendix 1; Appendix 2
PRESCRIPTION MEDICINES CODE OF PRACTICE AUTHORITY Constitution and ProcedureIndex
Record Nr. UNINA-9910450500603321
London, : BMJ Books, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The textbook of pharmaceutical medicine [[electronic resource]]
The textbook of pharmaceutical medicine [[electronic resource]]
Edizione [4th ed. /]
Pubbl/distr/stampa London, : BMJ Books, 2002
Descrizione fisica 1 online resource (896 p.)
Disciplina 615.1
Altri autori (Persone) GriffinJ. P (John Parry)
O'GradyJohn
Collana New York Academy of Sciences
Soggetto topico Pharmaceutical chemistry
Pharmacology
ISBN 1-280-19787-0
9786610197873
1-4051-4606-0
1-4237-1777-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Contents; Contributors; Preface; Acknowledgements; The editors; 1: Discovery of new medicines; 2: Pharmaceutical development; 3: Toxicity testing; 4: Exploratory development; 5: Clinical pharmacokinetics; 6: Clinical trials and good clinical practice; 7: Medical statistics; 8: Development of medicines: full development; 9: The medical department; 10: Medical marketing; 11: Information and promotion; 12: The supply of unlicensed medicines for particular patient use; 13: Legal and ethical issues relating to medicinal products; 14: The safety of medicines
15: The development of the control of human medicines in Europe from classical times to the year 200016: Technical requirements for registration of pharmaceuticals for human use: the ICH process and the common technical document; 17: The regulation of drug products by the United States Food and Drug Administration; 18: The US FDA in the drug development, evaluation and approval process; 19: Regulatory and clinical trial systems in Japan; 20: Economics of healthcare; 21: Controls on NHS medicines prescribing and expenditure in the UK (a historical perspective); Appendix 1; Appendix 2
PRESCRIPTION MEDICINES CODE OF PRACTICE AUTHORITY Constitution and ProcedureIndex
Record Nr. UNINA-9910783139403321
London, : BMJ Books, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The textbook of pharmaceutical medicine [[electronic resource]]
The textbook of pharmaceutical medicine [[electronic resource]]
Edizione [4th ed. /]
Pubbl/distr/stampa London, : BMJ Books, 2002
Descrizione fisica 1 online resource (896 p.)
Disciplina 615.1
Altri autori (Persone) GriffinJ. P (John Parry)
O'GradyJohn
Collana New York Academy of Sciences
Soggetto topico Pharmaceutical chemistry
Pharmacology
ISBN 1-280-19787-0
9786610197873
1-4051-4606-0
1-4237-1777-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Contents; Contributors; Preface; Acknowledgements; The editors; 1: Discovery of new medicines; 2: Pharmaceutical development; 3: Toxicity testing; 4: Exploratory development; 5: Clinical pharmacokinetics; 6: Clinical trials and good clinical practice; 7: Medical statistics; 8: Development of medicines: full development; 9: The medical department; 10: Medical marketing; 11: Information and promotion; 12: The supply of unlicensed medicines for particular patient use; 13: Legal and ethical issues relating to medicinal products; 14: The safety of medicines
15: The development of the control of human medicines in Europe from classical times to the year 200016: Technical requirements for registration of pharmaceuticals for human use: the ICH process and the common technical document; 17: The regulation of drug products by the United States Food and Drug Administration; 18: The US FDA in the drug development, evaluation and approval process; 19: Regulatory and clinical trial systems in Japan; 20: Economics of healthcare; 21: Controls on NHS medicines prescribing and expenditure in the UK (a historical perspective); Appendix 1; Appendix 2
PRESCRIPTION MEDICINES CODE OF PRACTICE AUTHORITY Constitution and ProcedureIndex
Record Nr. UNINA-9910825628603321
London, : BMJ Books, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui