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 | ||
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Lo trovi qui: Univ. Federico II | ||
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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 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
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 | ||
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Lo trovi qui: Univ. Federico II | ||
|
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 | ||
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Lo trovi qui: Univ. Federico II | ||
|
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 | ||
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Lo trovi qui: Univ. Federico II | ||
|
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 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
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 | ||
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Lo trovi qui: Univ. Federico II | ||
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